510(k) K922552 ยท DQO Catheter, Intravascular, Diagnostic
MORSE(R) ANGIOGRAPHIC CATHETERS
| Applicant | North American Instrument Corp., Glens Falls NY, US |
| Decision | Substantially Equivalent, Mar 3, 1993 |
| Received | May 29, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922552
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.