510(k) K053251 ยท DQX Wire, Guide, Catheter
TECHDEVICE GUIDEWIRE
| Applicant | Techdevice Corporation, Watertown MA, US |
| Decision | Substantially Equivalent, Mar 8, 2006 |
| Received | Nov 21, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053251
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.