USAMMDA Announces FDA 510 (k) Clearance of Rapid Diagnostic Test for COVID-19

By militarymedical on July 1, 2024Comments Off on USAMMDA Announces FDA 510 (k) Clearance of Rapid Diagnostic Test for COVID-19

The BioFire COVID-19 Test 2 is an in vitro diagnostic test used in conjunction with the BioFire FilmArray instrument to analyze nasopharyngeal swab specimens from symptomatic individuals suspected of COVID-19 by their healthcare provider. (Photo courtesy of BioFire Defense)