510(k) K240578 · DTK Filter, Intravascular, Cardiovascular
VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter System
| Applicant | B.Braun Medical, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jul 31, 2024 |
| Received | Mar 1, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240578
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.