510(k) K863724 ยท DSI Detector And Alarm, Arrhythmia
MODEL 6000 AMBULATORY ECG ANALYSIS SYSTEM
| Applicant | Oxford Medilog, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Nov 20, 1986 |
| Received | Sep 23, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863724
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.