1. FDA authorizes first at-home COVID-19 test kit as cases surge nationwide  KHOU 11
  2. FDA approves first at-home COVID-19 test that delivers results in 30 minutes  Daily Mail
  3. FDA Allows 1st Rapid Virus Test That Gives Results at Home  Snopes.com
  4. Lucira Health's At-Home Covid Test, Explained  Bloomberg
  5. FDA greenlights first all-in-one home COVID-19 test, with results in 30 minutes  FierceBiotech
  6. View Full coverage on Google News
The FDA approved the single-use test kit from Lucira Health on Tuesday, marking an important step in US efforts to expand testing options for COVID-19 beyond health care facilities and testing sites.The FDA approved the single-use test kit from Lucira Health on Tuesday, marking an important step in US efforts to expand testing options for COVID-19 beyond health care facilities and testing sites.

FDA approves first at-home COVID-19 test that delivers results in 30 minutes | Daily Mail Online

Today, the U.S. Food and Drug Administration announced that they've issued an emergency use authorization (EUA) for the first at-home COVID-19 diagnostic test, meaning that you'll be able to test yourself for the novel virus in the comfort of your own home.Today, the U.S. Food and Drug Administration announced that they've issued an emergency use authorization (EUA) for the first at-home COVID-19 diagnostic test, meaning that you'll be able to test yourself for the novel virus in the comfort of your own home.

Bloomberg - Are you a robot?

Lucira's molecular testing kit allows individuals to collect their own nasal sample and insert it into a device that provides results in under 30 minutes. The company is aiming to sell the single-use tests for roughly $50.Lucira's molecular testing kit allows individuals to collect their own nasal sample and insert it into a device that provides results in under 30 minutes. The company is aiming to sell the single-use

FDA authorizes first COVID-19 test for self-testing at home | MobiHealthNews

Some experts think that at-home testing can stop coronavirus outbreaks, and that the government should have been doing more to produce the tests.Some experts think that at-home testing can stop coronavirus outbreaks, and that the government should have been doing more to produce the tests.

Can You Test At Home for Coronavirus? - The Atlantic

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Innovative Testing Strategies for COVID-19 Containment | Infection Control Today

The FDA has authorized its first all-in-one COVID-19 diagnostic that allows people to test themselves within their own home, from a swab to a result in about 30 minutes.The FDA has authorized its first all-in-one COVID-19 diagnostic that allows people to test themselves within their own home, from a swab to a result in about 30 minutes.

FDA greenlights first all-in-one home COVID-19 test, with results in 30 minutes | FierceBiotech

WASHINGTON: US regulators on Tuesday (Nov 17) allowed emergency use of the first rapid coronavirus test that can be performed and developed ...WASHINGTON: US regulators on Tuesday (Nov 17) allowed emergency use of the first rapid coronavirus test that can be performed and developed ...

US approves first COVID-19 test kit that gives results at home - CNA

The U.S. Food and Drug Administration (FDA) has issued an emergency use authorization (EUA) for the Lucira COVID-19 All-In-One Test Kit: the first COVID-19 diagnostic test for self-testing at home.The U.S. Food and Drug Administration (FDA) has issued an emergency use authorization (EUA) for the Lucira COVID-19 All-In-One Test Kit: the first COVID-19 diagnostic test for self-testing at home.

FDA authorises first COVID-19 home self-testing kit

The 30 minutes test allows users to swab themselves to collect a nasal sample and then provide the test result at homeThe 30 minutes test allows users to swab themselves to collect a nasal sample and then provide the test result at home

FDA Approves 1st COVID-19 Rapid Test Kit That Gives Results at Home in 30 Minutes

Lucira Health’s prescription COVID-19 All-In-One Test Kit can be performed entirely at home — or in point-of-care settings — with results in 30 minutes or less.Lucira Health’s prescription COVID-19 All-In-One Test Kit can be performed entirely at home — or in point-of-care settings — with results in 30 minutes or less.

FDA Clears First Rapid At-Home COVID Test

The home testing kit can deliver results in 30 minutes and is considered more accurate than a rapid antigen testThe home testing kit can deliver results in 30 minutes and is considered more accurate than a rapid antigen test

First Covid tests that give immediate result to user at home authorised in US | The Independent

Late yesterday the U.S. Food and Drug Administration (FDA) authorized the first prescription molecular diagnostic test for COVID-19 that can be perforLate yesterday the U.S. Food and Drug Administration (FDA) authorized the first prescription molecular diagnostic test for COVID-19 that can be perfor

FDA Authorizes First Prescription at Home Molecular Test for COVID-19 | Business Wire

The first at-home rapid coronavirus test has been approved by the FDA, according to CBS Money Watch. The test created by Lucira Health, a California manufacturer, takes about 30 minutes to take and receive the results. The first at-home rapid coronavirus test has been approved by the FDA, according to CBS Money Watch. The test created by Lucira Health, a California manufacturer, takes about 30 minutes to take and…

First at-home rapid coronavirus test approved by the FDA | KLAS

The Lucira COVID-19 All-In-One Test Kit is expected to provide results in 30 minutes or less. Its approval could help alleviate the strain on the nation's precarious coronavirus testing system.The Lucira COVID-19 All-In-One Test Kit is expected to provide results in 30 minutes or less. Its approval could help alleviate the strain on the nation's precarious coronavirus testing system.

FDA Approves 1st At-Home Coronavirus Test : Coronavirus Updates : NPR

The U.S. Food and Drug Administration said on Tuesday it had approved the first COVID-19 self-testing kit for home use that provides results within 30 minutes. The single-use test, made by Lucira Health, has been given emergency use authorization for home use with self-collected nasal swab samples in individuals agedThe U.S. Food and Drug Administration said on Tuesday it had approved the first COVID-19 self-testing kit for home use that provides results within 30 minutes. The single-use test, made by Lucira Health, has been given emergency use authorization for home use with self-collected nasal swab samples in individuals aged

FDA Approves First COVID-19 Test Kit for Home Use | Hamodia.com

The FDA has granted emergency authorization to a Covid-19 test that can be taken at home and will quickly provide the results, the agency said Tuesday.The Lucira COVID-19 All-In-One Test Kit requires a prescription and works in about 30 minutes, the FDA says.

FDA authorizes first at-home Covid-19 test that gives users results quickly

'Today's transparency action is just one of a number of steps we are taking to ensure public confidence in our EUA review process for drugs and biological products, especially any potential Covid vaccines,' FDA Commissioner Stephen Hahn said'Today's transparency action is just one of a number of steps we are taking to ensure public confidence in our EUA review process for drugs and biological products, especially any potential Covid vaccines,' FDA Commissioner Stephen Hahn said

US to make emergency use authorisation data public for coronavirus vaccines

FDA grants the first emergency use authorization for at-home rapid coronavirus testsFDA grants the first emergency use authorization for at-home rapid coronavirus tests

Coronavirus: FDA has approved an at-home rapid COVID-19 test - Deseret News

At-home testing is now available for those who wish to take a coronavirus test from inside their homes, Chicago’s top public health official said Wednesday.At-home testing is now available for those who wish to take a coronavirus test from inside their homes, Chicago’s top public health official said Wednesday.

How You Can Get an At-Home Coronavirus Test and What You Should Do When You Get One – NBC Chicago

Emergency use authorised for do-it-yourself test, with results as soon as 11 minutes.Emergency use authorised for do-it-yourself test, with results as soon as 11 minutes.

Covid 19 coronavirus: First home-test kit with rapid results approved - NZ Herald

Accurate, inexpensive, rapid tests hold the key to getting the pandemic under control. Accurate, inexpensive, rapid, home tests are even better. RT-LAMP tests aren’t based on some new breakthrough technology, though.Accurate, inexpensive, rapid tests hold the key to getting the pandemic under control. Accurate, inexpensive, rapid, home tests are even better. RT-LAMP tests aren’t based on some new breakthrough technology, though.

Covid-19: What you need to know today - india news - Hindustan Times

The Food and Drug Administration (FDA) announced Tuesday the emergency approval of the first COVID-19 test that can be done fully at home. Lucira Health'sThe nasal swab test kit from Lucira Health can only be used at-home on prescription by a healthcare provider, the FDA said.

The FDA announced emergency approval of the first COVID-19 self-test that can be done fully at home. It provides results in 30 minutes. | Business Insider India

The test, developed by the California-based company Lucira Health, requires a prescription from a health care provider, and people younger than 14 also cannot perform the test on themselves.   The test, developed by the California-based company Lucira Health, requires a prescription from a health care provider, and people younger than 14 also cannot perform the test on themselves.  

US FDA authorizes first at-home coronavirus test | ABS-CBN News

The U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for the first COVID-19 at-home diagnostic self-test ...The U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for the first COVID-19 at-home diagnostic self-test that provides rapid results. What...

CVS Corporation (NYSE:CVS), Moderna, Inc. (MRNA) - FDA Gives Nod To First COVID-19 At-Home Rapid Test | Benzinga

A rapid do-it-yourself coronavirus test could be a game-changer.A rapid do-it-yourself coronavirus test could be a game-changer.

‘Game-Changer’: FDA Authorizes First At-Home Coronavirus Test – CBS Pittsburgh

You can now get tested for COVID-19 without having to leave home, and U.S. regulators announced Tuesday that you’ll soon be able to get tested without even...You can now get tested for COVID-19 without having to leave home, and U.S. regulators announced Tuesday that you’ll soon be able to get tested without even having to mail a sample to a lab — but there are several factors to consider as you weigh your options.  Look at the testing turnaround time, the convenience, the cost and whether…

At-Home COVID-19 Testing Is Convenient, But Here’s What Else to Consider – NBC4 Washington

A coronavirus at-home testing kit from Lucira that offers results in 30 minutes is the first-ever approved by the FDA, which issued an emergency use authorization. It works via self-administered nasal swab which is then placed in the test unit. CNBC reports: “Produced by a privately held, California-based biotech company, Lucira Health, the kit is […]

Coronavirus At-Home Testing Kit is First-Ever Approved by FDA and Gives Results in 30 Minutes - Towleroad Gay News

The at-home kit administers what's known as a molecular diagnostic test — which searches for the virus's RNA fingerprint.

FDA OKs 1st rapid virus test that allows results at home

US Food and Drug Administration approved on Tuesday emergency use of the first-ever COVID-19 test that can be performed entirely at home This is the first test that can be fully self-administered and provides results within 30 minutes or less, according to the FDA. The test can be performed by collecting a sample, either a nasal swab or saliva, and swirling it in a vial of laboratory solution. This solution is then plugged into a portable device with a light-up display, which shows whether the person is negative or positive for the virus after 30 minutes or less. The test will be available by prescription to individuals aged 14 years and older who have symptoms for COVID-19. A ...US Food and Drug Administration approved on Tuesday emergency use of the first-ever COVID-19 test that can be performed entirely at home This is the first test that can be fully self-administered and provides results within 30 minutes or less, according to the FDA. The test can be performed by collecting a sample, either a nasal swab or saliva, and swirling it in a vial of laboratory solution. This solution is then plugged into a portable device with a light-up display, which shows whether the person is negative or positive for the virus after 30 minutes or less. The test will be available by prescription to individuals aged 14 years and older who have symptoms for COVID-19. A ...

SAMAA - US approves first COVID-19 test that gives results at home

The FDA on Tuesday granted emergency authorization to the first at-home, self-testing coronavirus rapid result kit.The FDA on Tuesday granted emergency authorization to the first at-home, self-testing coronavirus rapid result kit.

The Food and Drug Administration on Tuesday gave emergency use authorization for a 30-minute COVID-19 test you can take entirely at home. The test, by Lucira Health, requires a prescription, and children under 14 must be given the test at a clinic or pharmacy. It's the first test approved in the U.S. that can be completed at home.To use the test, people swab the inside of both nostrils then put the sample in the vial on a battery-powered machine, which lights up with the results within half an hour. Lucira, based in California, says the test should cost $50 or less.> The first FDA approved for a complete at-home COVID test: The FDA granted emergency authorization to the 30-minute test kit from Lucira Health, a California manufacturer. pic.twitter.com/syiXirnRyc> > — Amichai Stein (@AmichaiStein1) November 18, 2020Lucira's home test works in a similar way to the extremely accurate lab ones that rely on a technique called polymerase chain reaction (PCR). Instead of PCR, Lucira uses a method called loop mediated amplification reaction (LAMP), The New York Times reports, which "repeatedly copies genetic material until it reaches detectable levels, making it possible to identify the virus even when it is present at only very low levels in the respiratory tract."Lucira says its LAMP test was able to detect 94 percent of COVID-19 cases confirmed by a PCR test and identified 98 percent of healthy test takers. People who test positive are expected to self-isolate for 10 days.More stories from theweek.com The class folly of canceling student loans Let's appreciate how extraordinary the vaccines are Donald Trump's future is a Prairie Home CompanionThe Food and Drug Administration on Tuesday gave emergency use authorization for a 30-minute COVID-19 test you can take entirely at home. The test, by Lucira Health, requires a prescription, and children under 14 must be given the test at a clinic or pharmacy. It's the first test approved in the U.S. that can be completed at home.To use the test, people swab the inside of both nostrils then put the sample in the vial on a battery-powered machine, which lights up with the results within half an hour. Lucira, based in California, says the test should cost $50 or less.> The first FDA approved for a complete at-home COVID test: The FDA granted emergency authorization to the 30-minute test kit from Lucira Health, a California manufacturer. pic.twitter.com/syiXirnRyc> > — Amichai Stein (@AmichaiStein1) November 18, 2020Lucira's home test works in a similar way to the extremely accurate lab ones that rely on a technique called polymerase chain reaction (PCR). Instead of PCR, Lucira uses a method called loop mediated amplification reaction (LAMP), The New York Times reports, which "repeatedly copies genetic material until it reaches detectable levels, making it possible to identify the virus even when it is present at only very low levels in the respiratory tract."Lucira says its LAMP test was able to detect 94 percent of COVID-19 cases confirmed by a PCR test and identified 98 percent of healthy test takers. People who test positive are expected to self-isolate for 10 days.More stories from theweek.com The class folly of canceling student loans Let's appreciate how extraordinary the vaccines are Donald Trump's future is a Prairie Home Companion

FDA authorizes rapid COVID-19 test you can complete at home

It allows people to test themselves and get the results at home, within 30 minutes.It allows people to test themselves and get the results at home, within 30 minutes.

FDA authorizes 1st fully at-home COVID-19 test | Live Science

The Food and Drug Administration has approved the first rapid at-home COVID-19 test that could have results returned within an hour.The FDA issued an emergency use authorization on Tuesday, Nov. 17 for the The Food and Drug Administration has approved the first rapid at-home COVID-19 test that could have results returned within an hour.The FDA issued an emergency use authorization on Tuesday, Nov. 17 for the

COVID-19: FDA Approves First Rapid At-Home Test | Yorktown Daily Voice

An Emeryville biotech company, Lucira Health, started by four Cal graduate students is releasing a COVID-19 home test kit under emergency FDA approval.A Bay Area-based biotech company just got emergency FDA approval for their COVID-19 at-home test kit. Here's how it works:

1st COVID-19 at-home test delivers positive results in 11 minutes - here's California company's kit works | abc7news.com

The Food and Drug Administration has approved the first rapid coronavirus test kit that can be performed at home, issuing an emergency use authorization to manufacturer Lucira Health late on Tuesday.The Food and Drug Administration has approved the first rapid coronavirus test kit that can be performed at home, issuing an emergency use authorization to manufacturer Lucira Health late on Tuesday.

FDA Issues First Emergency Use Authorization for At-Home Coronavirus Test

The new home administered rapid COVID-19 test is manufactured in Emeryville and could be a game changer.The new home administered rapid COVID-19 test is manufactured in Emeryville and could be a game changer.

The molecular single-use test provides a positive or negative result in 30 minutes after swirling a nasal swab in a vial linked to a portable test unit. The Food and Drug Administration’s emergency authorization announced Tuesday would require a prescription to access the kit. The agency mandated health providers to report all home test results.

FDA approves first COVID-19 home test - Health - WORLD

Costco, Albertson's, Safeway, Vons and Walmart are among the many companies offering at-home COVID-19 tests. Costco, Albertson's, Safeway, Vons and Walmart are among the many companies offering at-home COVID-19 tests.

1st COVID-19 at home self-test authorized by FDA as cases surge in US | GMA