510(k) K860024 ยท DSI Detector And Alarm, Arrhythmia
FUKUDA DENSHI CARDIMAX FCP-211
| Applicant | Brentwood Instruments, Inc., Torrange CA, US |
| Decision | Substantially Equivalent, Mar 31, 1986 |
| Received | Jan 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860024
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.