510(k) K914352 ยท DYB Introducer, Catheter
CORDIS OBTURATOR
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Nov 22, 1991 |
| Received | Sep 30, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914352
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.