510(k) K925444 ยท DYG Catheter, Flow Directed
CARDIAC OUTPUT PULMONARY ARTERY CATHETER & MONITOR
| Applicant | Ami-Med Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Jul 19, 1993 |
| Received | Oct 28, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925444
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.