510(k) K914312 ยท DQO Catheter, Intravascular, Diagnostic
SCIMED 7FR AND 8FR TRIGUIDE GUIDING CATHETERS
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Nov 22, 1991 |
| Received | Sep 26, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914312
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.