510(k) K922060 ยท DQX Wire, Guide, Catheter
.25' ULTRA-SELECT GUIDEWIRE
| Applicant | Microvena Corp., Vadnais Heights MN, US |
| Decision | Substantially Equivalent, Feb 23, 1993 |
| Received | May 4, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922060
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.