ClearanceBrief
510(k) K884106 ยท DSI Detector And Alarm, Arrhythmia

SUPERVISORY TELEMETRY ARRHYTHMIA TERMINAL

ApplicantSiemens Medical Solutions USA, Inc., Iselin NJ, US
DecisionSubstantially Equivalent, Mar 6, 1989
ReceivedSep 29, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884106

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.