510(k) K920743 ยท DSI Detector And Alarm, Arrhythmia
DUAL LEAD (ECG1 & ECG2) ARRHYTHMIA ANALYSIS
| Applicant | Nihon Kohden America, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 3, 1992 |
| Received | Feb 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920743
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.