510(k) K961917 ยท DQX Wire, Guide, Catheter
MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX)
| Applicant | Medtronics Interventional Vascular, San Diego CA, US |
| Decision | Substantially Equivalent, Nov 20, 1996 |
| Received | May 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961917
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.