510(k) K925852 ยท DQX Wire, Guide, Catheter
TERUMO CORONARY GUIDE WIRE
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Jun 10, 1993 |
| Received | Nov 17, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925852
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.