510(k) K944422 ยท DSI Detector And Alarm, Arrhythmia
BSM-8800A BEDSIDE MONITOR
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, May 24, 1995 |
| Received | Aug 16, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K944422
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.