510(k) K950094 ยท DQY Catheter, Percutaneous
SCIMED 6 FRENCH MICRO-MAX(TM) GUIDE CATHETER
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Mar 3, 1995 |
| Received | Jan 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950094
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.