510(k) K914092 ยท DSI Detector And Alarm, Arrhythmia
BSM-2100A CONFIGURED PATIENT MONITOR
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, May 28, 1992 |
| Received | Sep 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914092
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.