510(k) K953909 ยท DQY Catheter, Percutaneous
SCIMED 6 FRENCH MICRO-MAX GUIDE CATHETER
| Applicant | Scimed, Maple Grove MN, US |
| Decision | Substantially Equivalent, Nov 13, 1995 |
| Received | Aug 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953909
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.