ClearanceBrief
510(k) K960418 ยท DSI Detector And Alarm, Arrhythmia

EAGLE PATIENT MONITOR

ApplicantMarquette Electronics, Inc., Milwaukee WI, US
DecisionSubstantially Equivalent, Oct 2, 1996
ReceivedJan 29, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960418

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.