510(k) K881604 ยท DTK Filter, Intravascular, Cardiovascular
VENA CAVA FILTER
| Applicant | Vena-Tech, Inc., Brookline MA, US |
| Decision | Substantially Equivalent, Mar 10, 1989 |
| Received | Apr 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881604
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.