510(k) K132623 ยท DQX Wire, Guide, Catheter
MEDTRONIC CONFIDA BRECKER CURVE GUIDEWIRE
| Applicant | Medtronic, Santa Rosa CA, US |
| Decision | Substantially Equivalent, Dec 19, 2013 |
| Received | Aug 22, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132623
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.