510(k) K243872 ยท QVF Simple Point-Of-Care Device To Directly Detect Sars-Cov-2 Viral Targets From Clinical Specimens In Near-Patient Settings
BD Veritor System for SARS-CoV-2
| Applicant | Becton, Dickinson and Company, Sparks MD, US |
| Decision | Substantially Equivalent, Jun 16, 2025 |
| Received | Dec 17, 2024 |
| Type | Dual Track |
| FDA record | Open on fda.gov |
Recalls that name K243872
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.