510(k) K973845 ยท DQX Wire, Guide, Catheter
CORDIS HYDRONOL STEERABLE GUIDEWIRE
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Jan 5, 1998 |
| Received | Oct 8, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K973845
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.