510(k) K831274 ยท DSI Detector And Alarm, Arrhythmia
WLECTROCARDIOGRAPH ECG-7204
| Applicant | Nihon Kohden America, Inc., Foothill CA, US |
| Decision | Substantially Equivalent, Oct 27, 1983 |
| Received | Apr 19, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831274
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.