510(k) K780432 ยท DSI Detector And Alarm, Arrhythmia
ARRHYTHMIA PROGRAM MODULE
| Applicant | Midwest Analog & Digital, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 26, 1978 |
| Received | Mar 17, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780432
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.