510(k) K181001 ยท DQX Wire, Guide, Catheter
Medtronic Confida Brecker Guidewire
| Applicant | Medtronic Core Valve, LLC, Galway, IE |
| Decision | Substantially Equivalent, May 3, 2018 |
| Received | Apr 16, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181001
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.