510(k) K953265 ยท DQY Catheter, Percutaneous
SCIMED ANGIOGRAPHIC KITS
| Applicant | Scimed Life Systems, Inc., Maple Grove MN, US |
| Decision | Substantially Equivalent, Jan 16, 1996 |
| Received | Jul 13, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953265
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.