510(k) K894633 ยท DQX Wire, Guide, Catheter
CORDIS STEERABLE COATED GUIDEWIRE
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Oct 17, 1989 |
| Received | Jul 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894633
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.