510(k) K896308 ยท DQO Catheter, Intravascular, Diagnostic
CORDIS SHUTTLE CATHETER
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Mar 28, 1990 |
| Received | Nov 1, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896308
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.