510(k) K090274 ยท DQX Wire, Guide, Catheter
MICRUS ONE 2 ONE GUIDEWIRE AND SOFT GUIDEWIRE
| Applicant | Micrus Endovascular Corporation, San Jose CA, US |
| Decision | Substantially Equivalent, Mar 3, 2009 |
| Received | Feb 4, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090274
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.