510(k) K173532 ยท DQX Wire, Guide, Catheter
Raider Guidewire
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 15, 2017 |
| Received | Nov 15, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173532
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.