510(k) K954423 ยท DQO Catheter, Intravascular, Diagnostic
ANGIOPTIC ANGIOGRAPHIC CATHETER
| Applicant | AngioDynamics, Inc., Glens Falls NY, US |
| Decision | Substantially Equivalent, Dec 1, 1995 |
| Received | Sep 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954423
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.