ClearanceBrief
510(k) K071889 ยท DSI Detector And Alarm, Arrhythmia

DATEX-OHMEDA S/5 CRITICAL CARE MONITOR WITH L-ICU05 AND L-ICU05A SOFTWARE

ApplicantGE Healthcare, Needham MA, US
DecisionSubstantially Equivalent, May 19, 2008
ReceivedJul 9, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071889

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.