510(k) K923134 ยท DQX Wire, Guide, Catheter
CORDIS STEERABLE GUIDEWIRE
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Oct 26, 1992 |
| Received | Jun 29, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923134
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.