510(k) K003964 ยท DTK Filter, Intravascular, Cardiovascular
TRAPEASE PERMANENT VENA FILTER AND INTRODUCTION KIT, MODELS 466-P306A AND 466-P306B
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Substantially Equivalent, Jan 19, 2001 |
| Received | Dec 22, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K003964
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.