510(k) K935654 ยท DQO Catheter, Intravascular, Diagnostic
SCIMED 10 FR. LG. LUMEN TRIGUIDE PLUS(TM) GUID CATH
| Applicant | Scimed Life Systems, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Feb 22, 1994 |
| Received | Nov 24, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935654
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.