510(k) K961139 ยท DSI Detector And Alarm, Arrhythmia
EAGLE PATIENT MONITOR MODEL 3000/3100
| Applicant | Marquette Electronics, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Aug 9, 1996 |
| Received | Mar 21, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961139
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.