510(k) K962291 ยท DSI Detector And Alarm, Arrhythmia
SIEMENS SC9000/SC9015 BEDSIDE MONITORING SYSTEM
| Applicant | Siemens Medical Solutions USA, Inc., Danvers MA, US |
| Decision | Substantially Equivalent, Jan 29, 1997 |
| Received | Jun 14, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962291
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.