510(k) K954852 ยท DSI Detector And Alarm, Arrhythmia
SOLAR 9000 ANESTHESIA INFORMATION MONITOR
| Applicant | Marquette Electronics, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, May 29, 1996 |
| Received | Oct 23, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954852
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.