510(k) K952430 ยท DQX Wire, Guide, Catheter
FINESSE GUIDEWIRE CORONARY
| Applicant | Flexmedics, Minnetonka MN, US |
| Decision | Substantially Equivalent, Aug 18, 1995 |
| Received | May 24, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952430
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.