510(k) K232434 · PSZ Devices Detecting Influenza A, B, And C Virus Antigens
BD Veritor System for Rapid Detection of Flu A+B CLIA Waived Kit
| Applicant | Bd, Sparks MD, US |
| Decision | Substantially Equivalent, Dec 5, 2023 |
| Received | Aug 11, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232434
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.