510(k) K895437 ยท DQO Catheter, Intravascular, Diagnostic
SCIMED CORONARY GUIDING CATHETER
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jun 28, 1990 |
| Received | Sep 8, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895437
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.