510(k) K072354 ยท OCY Endoscopic Guidewire, Gastroenterology-Urology
GUIDEWIRE, MODEL G-V220-3527S AND OTHERS
| Applicant | Accellent, Inc., Wilmington MA, US |
| Decision | Substantially Equivalent, Dec 7, 2007 |
| Received | Aug 22, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072354
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.