510(k) K163444 ยท DQX Wire, Guide, Catheter
Spectre guidewire
| Applicant | Vascular Solutions, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jan 6, 2017 |
| Received | Dec 8, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K163444
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.