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15.04.2022 / 21:17

FDA authorizes COVID breath test for emergency use

The US Food and Drug Administration (FDA) yesterday authorized for emergency use the first COVID-19 test based on breath samples, a system that looks for chemical signatures of infection and can provide a result in about 3 minutes.

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First breath testing device to detect Covid-19 infection authorised for emergency use. Details here

AP report.

Jeff Shuren India covid-19 testing Health

1st COVID-19 breath test given emergency use authorization by FDA

FILE -FDA logo and protective face masks are seen in this illustration photo taken in Krakow, Poland on Jan. 11, 2022.

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4th at-home COVID-19 test gets emergency use authorization from FDA

WASHINGTON - The U.S.

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FDA OKs COVID-19 rapid test; CDC talks testing guidance

The US Food and Drug Administration (FDA) has granted an emergency use authorization (EUA) for a rapid COVID-19 test developed by Abbott Laboratories.

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COVID-19

United States	Cases: 46 252 513 Deaths: 750 423 Recovered: 0
India	Cases: 34 321 025 Deaths: 459 652 Recovered: 0
Brazil	Cases: 21 835 785 Deaths: 608 235 Recovered: 0
United Kingdom	Cases: 9 215 683 Deaths: 141 607 Recovered: 0
Russia	Cases: 8 494 589 Deaths: 237 619 Recovered: 0

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