510(k) K914141 ยท DQO Catheter, Intravascular, Diagnostic
CORDIS DUAL LUMEN PRESSURE MONITORING CATHETER
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Oct 23, 1991 |
| Received | Sep 16, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914141
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.