510(k) K222478 · JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
BD Vacutainer® Luer-Lok Access Device, BD Vacutainer® Blood Transfer Device
| Applicant | Becton, Dickinson and Company, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Mar 10, 2023 |
| Received | Aug 16, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222478
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.