510(k) K053265 ยท DQX Wire, Guide, Catheter
MICRUS GUIDE WIRE, WATUSI 0.014
| Applicant | Micrus Endovascular Corporation, Sunnyvale CA, US |
| Decision | Substantially Equivalent, Apr 28, 2006 |
| Received | Nov 22, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053265
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 29, 2006 | Micrus Endovascular Corporation Micrus brand WATUSI Guidewire 0.014'' - Soft Tip, Catalog Number; WST 140205-00;
Distributed by Micrus Endovascular Corporation. San Jose, CA Terminated |
DQX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.