FDA clears Hologic’s Aptima SARS-CoV-2 assay
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Hologic's in vitro diagnostic test, Aptima SARS-CoV-2 assay. The post FDA clears Hologic’s Aptima SARS-CoV-2 assay appeared first on Medical Device Network.

The post FDA clears Hologic’s Aptima SARS-CoV-2 assay appeared first on Medical Device Network.