510(k) K232570 · DQX Wire, Guide, Catheter
Steerant Super Stiff Guidewire
| Applicant | Medtronic Vascular, Santa Rosa CA, US |
| Decision | Substantially Equivalent, Oct 24, 2023 |
| Received | Aug 24, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232570
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.