510(k) K141218 ยท DQX Wire, Guide, Catheter
ZIGIWIRE MODE2 GUIDEWIRE WIRE SYSTEM, ZIGIWIRE MODE3 GUIDEWIRE WIRE SYSTEM
| Applicant | Vadiswire Corporation, Kirkland WA, US |
| Decision | Substantially Equivalent, Dec 18, 2014 |
| Received | May 12, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141218
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.