510(k) K964033 ยท DQO Catheter, Intravascular, Diagnostic
3F ANGIOPTIC ANGIOGRAPHIC CATHETER
| Applicant | AngioDynamics, Inc., Queensburgy NY, US |
| Decision | Substantially Equivalent, May 6, 1997 |
| Received | Oct 8, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964033
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.