510(k) K120863 ยท DQX Wire, Guide, Catheter
WHOLEY GUIDE WIRE SYSTEM
| Applicant | Covidien, LLC, Plymouth MN, US |
| Decision | Substantially Equivalent, Apr 19, 2012 |
| Received | Mar 22, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120863
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.