510(k) K863137 ยท DQO Catheter, Intravascular, Diagnostic
TERUMO RADIFOCUS ANGIOGRAPHIC CATHETER
| Applicant | Terumo Medical Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Oct 10, 1986 |
| Received | Aug 15, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863137
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.