510(k) K923607 ยท KOD Catheter, Urological
RADIFOCUS GUIDE WIRE M
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Oct 2, 1992 |
| Received | Jul 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923607
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.