510(k) K223653 ยท PQA Vaginitis And Bacterial Vaginosis Nucleic Acid Detection System
BD Vaginal Panel
| Applicant | Becton, Dickinson and Company, Sparks MD, US |
| Decision | Substantially Equivalent, Mar 6, 2023 |
| Received | Dec 6, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223653
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.