510(k) K872241 ยท DSI Detector And Alarm, Arrhythmia
LIFESCOPE 12, BSM 8500A PATIENT MONITOR
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 30, 1987 |
| Received | Jun 11, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872241
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.