510(k) K873874 ยท DSI Detector And Alarm, Arrhythmia
CARDIOFAX-V ECG-8110A
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 7, 1988 |
| Received | Sep 22, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873874
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.