510(k) K960801 ยท DQO Catheter, Intravascular, Diagnostic
SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)
| Applicant | North American Instrument Corp., Glens Falls NY, US |
| Decision | Substantially Equivalent, Mar 29, 1996 |
| Received | Feb 27, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960801
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.