510(k) K124007 ยท DQX Wire, Guide, Catheter
SILVERSPEED HYDROPHILIC GUIDEWIRE, X-CELERATOR HYDROPHILIC EXCHANGE GUIDEWIRE, X-PEDION HYDROPHILIC GUIDEWIRE, MIRAGE HY
| Applicant | Micro Therapeutics, Inc. D/B/A: Ev3, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Mar 7, 2013 |
| Received | Dec 26, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K124007
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.