510(k) K896103 ยท DSI Detector And Alarm, Arrhythmia
MICRO FL 7400 AMBULATORY HOLTER/BP MONITOR
| Applicant | Advanced Medical Products, Inc., Liverpool NY, US |
| Decision | Substantially Equivalent, Jan 18, 1990 |
| Received | Oct 23, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896103
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.