510(k) K854018 ยท DQO Catheter, Intravascular, Diagnostic
ANGIOGRAPHY CATHETERS
| Applicant | Micor, Inc., Pittsburgh PA, US |
| Decision | Substantially Equivalent, Jan 16, 1986 |
| Received | Sep 30, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854018
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.