510(k) K011759 ยท OCY Endoscopic Guidewire, Gastroenterology-Urology
RADIUS NEXT GENERATION GUIDEWIRE
| Applicant | Radius Medical Technologies, Inc., Maynard MA, US |
| Decision | Substantially Equivalent, Aug 23, 2001 |
| Received | Jun 6, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011759
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.