510(k) K913576 ยท DSI Detector And Alarm, Arrhythmia
DATASCOPE MODEL VISA CENTRAL MONITOR
| Applicant | Accucore, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Jan 28, 1992 |
| Received | Aug 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913576
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.