510(k) K873680 ยท DSI Detector And Alarm, Arrhythmia
MODEL 6000FD AMBULATORY ECG ANALYSIS SYSTEM
| Applicant | Oxford Medilog, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Nov 23, 1987 |
| Received | Sep 14, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873680
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.