510(k) K924202 ยท DQX Wire, Guide, Catheter
RADIFOCUS(R) (CATHETER) GUIDE WIRE
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Nov 23, 1992 |
| Received | Aug 20, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924202
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.