510(k) K020316 ยท DQO Catheter, Intravascular, Diagnostic
CORDIS TRAPEASE PERMANENT VENA CAVA FILTER WITH THE VISEASE ANGIOGRAPHIC VESSEL DILATOR; MODELS 466-P306AU & 466-P306BU
| Applicant | Cordis Corp., Warren NJ, US |
| Decision | Substantially Equivalent, Mar 20, 2002 |
| Received | Jan 30, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020316
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.