510(k) K002212 ยท DQX Wire, Guide, Catheter
MIRAGE HYDROPHILIC GUIDEWIRE, MODEL 103-0608
| Applicant | Micro Therapeutics, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Aug 3, 2000 |
| Received | Jul 21, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K002212
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.