510(k) K896690 ยท DQO Catheter, Intravascular, Diagnostic
MODIFIED ANGIOGRAPHIC CATHETER
| Applicant | Novoste Corp., Aguadilla PR, US |
| Decision | Substantially Equivalent, Jan 24, 1990 |
| Received | Nov 28, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896690
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.