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)
| Date Taken: | 01.19.2022 |
| Date Posted: | 01.19.2022 11:19 |
| Photo ID: | 7015601 |
| VIRIN: | 220119-O-IE261-074 |
| Resolution: | 1584x907 |
| Size: | 319.62 KB |
| Location: | FORT DETRICK, MARYLAND, US |
| Web Views: | 87 |
| Downloads: | 18 |
This work, USAMMDA Announces FDA 510 (k) Clearance of Rapid Diagnostic Test for COVID-19 [Image 2 of 2], by Jeffrey Soares, identified by DVIDS, must comply with the restrictions shown on https://www.dvidshub.net/about/copyright.
USAMMDA Announces FDA 510 (k) Clearance of Rapid Diagnostic Test for COVID-19
USAMMDA receives Army Superior Unit Award for pandemic response
No keywords found.
