510(k) K982299 ยท DQO Catheter, Intravascular, Diagnostic
SPYGLASS 5 FR ANGIOGRAPHIC CATHETER
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Oct 19, 1998 |
| Received | Jul 1, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K982299
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.