510(k) K881905 ยท DSI Detector And Alarm, Arrhythmia
MODEL MICRO SI AMBULATORY ECG MONITOR
| Applicant | Advanced Medical Products, Inc., Liverpool NY, US |
| Decision | Substantially Equivalent, Aug 2, 1988 |
| Received | May 6, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881905
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.