510(k) K946356 ยท DQX Wire, Guide, Catheter
M-PATH NITINOL GUIDEWIRE
| Applicant | Microvena Corp., White Bear Lake MN, US |
| Decision | Substantially Equivalent, Mar 31, 1995 |
| Received | Dec 30, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946356
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.