510(k) K925342 ยท DQX Wire, Guide, Catheter
MEDTRONIC INTERVENTIONAL VASCULAR SHERPA GUIDEWIRE
| Applicant | Medtronics Interventional Vascular, Danvers MA, US |
| Decision | Substantially Equivalent, May 6, 1993 |
| Received | Oct 20, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925342
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.