510(k) K822718 ยท DSI Detector And Alarm, Arrhythmia
SERIES 7000 BEDSIDE PATIENT MONITOR
| Applicant | Marquette Electronics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 4, 1982 |
| Received | Sep 7, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822718
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.