The FDA Authorizes First COVID-19 Breath Test—Here’s What You Need to Know
According to a statement released by the agency, the test, performed by a device about the size of carry-on luggage, detects chemical compounds in breath samples associated with a SARS-CoV-2 infection. The FDA issued emergency use authorization for the device, permitting its operation by trained professionals and health care providers in doctors’ offices, hospitals, and mobile testing sites. From start to finish, test results can be available in less than three minutes.
This content is imported from YouTube. You may be able to find the same content in another format, or you may be able to find more information, at their web site.The efficacy of the innovative machine was studied among 2,409 individuals, including those with and without symptoms. The breathalyzer was shown to have 91.2% sensitivity and 99.3% specificity .
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