510(k) K955801 ยท DQX Wire, Guide, Catheter
RADIFOCUS GLIDEWIRE GT WITH GOLD COIL,GLIDEWIRE GOLD
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Feb 2, 1996 |
| Received | Dec 22, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955801
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.