510(k) K914007 ยท DQO Catheter, Intravascular, Diagnostic
CORDIS 5.2 FRENCH SUPER TORQUE PLUS CARDIO CATH
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Oct 18, 1991 |
| Received | Sep 9, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914007
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.