510(k) K150465 ยท DQX Wire, Guide, Catheter
Medtronic Confida Brecker Guidewire
| Applicant | Medtronic Core Valve, LLC, Santa Rosa CA, US |
| Decision | Substantially Equivalent, Aug 3, 2015 |
| Received | Feb 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150465
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.