510(k) K040592 ยท DQX Wire, Guide, Catheter
CORDIS STEER-IT DEFLECTING TIP GUIDEWIRE
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Dec 17, 2004 |
| Received | Mar 8, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040592
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.