ClearanceBrief
510(k) K190472 ยท PQA Vaginitis And Bacterial Vaginosis Nucleic Acid Detection System

Aptima CV/TV Assay

ApplicantHologic, Inc., San Diego CA, US
DecisionSubstantially Equivalent, May 16, 2019
ReceivedFeb 26, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K190472

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.