ClearanceBrief
510(k) K964624 ยท DSI Detector And Alarm, Arrhythmia

SIEMENS SC9000/SC9015 BEDSIDE MONITORING SYSTEM

ApplicantSiemens Medical Solutions USA, Inc., Danvers MA, US
DecisionSubstantially Equivalent, Sep 11, 1997
ReceivedNov 12, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964624

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.