510(k) K843731 ยท DSI Detector And Alarm, Arrhythmia
KENZ 80Z MARK II
| Applicant | Suzuken Co., Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 11, 1985 |
| Received | Sep 24, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843731
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.