510(k) K946204 ยท DQY Catheter, Percutaneous
SCIMED(R) TRIDUIGE(R) GUIDE CATHETERS
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Mar 13, 1995 |
| Received | Dec 21, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K946204
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.