510(k) K152765 ยท DTK Filter, Intravascular, Cardiovascular
VENATECH CONVERTIBLE VENA CAVA FILTER SYSTEM
| Applicant | B. Braun Interventional Systems, Inc., Bethlehem PA, US |
| Decision | Substantially Equivalent, Feb 26, 2016 |
| Received | Sep 24, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152765
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.