510(k) K823844 ยท DSI Detector And Alarm, Arrhythmia
HORIZON ECG SYSTEM
| Applicant | Beckman Instruments, Inc., Fullerton CA, US |
| Decision | Substantially Equivalent, Jan 10, 1985 |
| Received | Dec 21, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823844
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.