ClearanceBrief
510(k) K823585 ยท DSI Detector And Alarm, Arrhythmia

COMPUTER-AIDED ELECTROCARDIOGRAPH FCP-13

ApplicantBrentwood Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 6, 1983
ReceivedDec 6, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823585

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.