510(k) K943783 ยท DQY Catheter, Percutaneous
7 FRENCH LARGE LUMEN TRIGUIDE-PLUS
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Oct 13, 1994 |
| Received | Aug 3, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943783
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.