510(k) K000062 ยท DTK Filter, Intravascular, Cardiovascular
CORDIS TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Substantially Equivalent, Jul 7, 2000 |
| Received | Jan 10, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000062
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.