510(k) K970545 ยท DSI Detector And Alarm, Arrhythmia
DASH 1000 PATIENT MONITOR
| Applicant | Marquette Medical Systems, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, May 8, 1997 |
| Received | Feb 12, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970545
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.