510(k) K925411 ยท DSI Detector And Alarm, Arrhythmia
MODEL 2041-PC/ST CARDIAC TELEMETRY MONITOR
| Applicant | Accucore, Inc., Santa Ana CA, US |
| Decision | Substantially Equivalent, Feb 25, 1993 |
| Received | Oct 26, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925411
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.