ClearanceBrief
510(k) K760368 ยท DSI Detector And Alarm, Arrhythmia

MONITORING & STRESS TESTING EQUIPMENT

ApplicantAdvanced Medical, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 28, 1977
ReceivedAug 4, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760368

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.