510(k) K010083 ยท DTK Filter, Intravascular, Cardiovascular
TRAPEASE PERMANENT VENA CAVA FILTER AND INTRODUCTION KIT, MODEL 466-P306A
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Substantially Equivalent, Jun 6, 2001 |
| Received | Jan 11, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010083
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.