510(k) K911703 ยท DQO Catheter, Intravascular, Diagnostic
CORDIS 8 FRENCH 0.084 I.D. PTCA GUIDING CATHETER
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jun 28, 1991 |
| Received | Apr 16, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911703
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.