510(k) K860078 ยท DSI Detector And Alarm, Arrhythmia
MEDILOG 2500 SYSTEM
| Applicant | Oxford Medilog, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Feb 26, 1986 |
| Received | Jan 8, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860078
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.