ClearanceBrief
510(k) K842640 ยท DSI Detector And Alarm, Arrhythmia

SPACELABS ICR ARRHYTHMIA MASTER I HOLTER

ApplicantSpacelabs, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 4, 1984
ReceivedJul 10, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842640

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.