510(k) K053028 ยท OCY Endoscopic Guidewire, Gastroenterology-Urology
TECHDEVICE GUIDEWIRE
| Applicant | Techdevice Corporation, Watertown MA, US |
| Decision | Substantially Equivalent, Jan 31, 2006 |
| Received | Oct 27, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053028
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.