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    USAMMDA Announces FDA 510 (k) Clearance of Rapid Diagnostic Test for COVID-19 [Image 1 of 2]

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

    FORT DETRICK, MARYLAND, UNITED STATES

    01.19.2022

    Photo by Jeffrey Soares 

    Medical Research and Development Command

    USAMMDA's Warfighter Protection and Acute Care Project Management Office, along with its commercial partner BioFire Defense, announced the FDA's 510 (k) clearance for BioFire's COVID-19 Test 2, which helps to detect the presence of SARS-CoV-2, the virus that causes COVID-19, in approximately 45 minutes. (Photo courtesy of BioFire Defense)

    IMAGE INFO

    Date Taken: 01.19.2022
    Date Posted: 01.19.2022 11:19
    Photo ID: 7015600
    VIRIN: 220119-O-IE261-995
    Resolution: 2150x1783
    Size: 383.31 KB
    Location: FORT DETRICK, MARYLAND, US

    Web Views: 53
    Downloads: 9

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