510(k) K140695 ยท DQX Wire, Guide, Catheter
COUGAR GUIDEWIRE, ZINGER GUIDWIRE, THUNDER GUIDEWIRE, PROVIA GUIDEWIRE, INTUITION GUIDEWIRE
| Applicant | Medtronic, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Jun 12, 2014 |
| Received | Mar 19, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140695
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.