510(k) K980882 ยท DSI Detector And Alarm, Arrhythmia
SIEMENS SC 7000 & SC 9000 XL INFINITY MODULAR BEDSIDE MONITOR
| Applicant | Siemens Medical Solutions USA, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Jun 5, 1998 |
| Received | Mar 9, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980882
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.