510(k) K923696 ยท DQX Wire, Guide, Catheter
CORDIS VIERA GUIDEWIRE
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Feb 3, 1993 |
| Received | Jul 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923696
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.