510(k) K983632 ยท DSI Detector And Alarm, Arrhythmia
SIEMENS SC 8000 BEDSIDE MONITOR
| Applicant | Siemens Medical Solutions USA, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Nov 6, 1998 |
| Received | Oct 15, 1998 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K983632
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.