510(k) K802312 ยท DSI Detector And Alarm, Arrhythmia
CC101 ECG MONITORING SYSTEM
| Applicant | Anthro-Metrics Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 7, 1981 |
| Received | Sep 23, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802312
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.