510(k) K910722 ยท OCY Endoscopic Guidewire, Gastroenterology-Urology
450CM GUIDE WIRE FOR G.I. USE
| Applicant | Terumo Corp., Somerset NJ, US |
| Decision | Substantially Equivalent, Mar 21, 1991 |
| Received | Feb 20, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910722
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.