510(k) K943777 ยท DQY Catheter, Percutaneous
SCIMED 8 FRENCH BIG-MAX GUIDE CATHETER
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Oct 13, 1994 |
| Received | Aug 2, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943777
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.