ClearanceBrief
510(k) K243725 ยท PQA Vaginitis And Bacterial Vaginosis Nucleic Acid Detection System

BD Vaginal Panel

ApplicantBecton, Dickinson and Company, Sparks MD, US
DecisionSubstantially Equivalent, Dec 19, 2024
ReceivedDec 3, 2024
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K243725

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.