510(k) K965249 ยท DQO Catheter, Intravascular, Diagnostic
SPYGLASS ANGIOGRAPHIC CATHETER
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Feb 21, 1997 |
| Received | Dec 12, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965249
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.