ClearanceBrief
510(k) K842976 ยท DSI Detector And Alarm, Arrhythmia

BRENTWOOD EZ SCAN 200 AMBULATORY ECG

ApplicantBrentwood Instruments, Inc., Torrance CA, US
DecisionSubstantially Equivalent, Mar 1, 1985
ReceivedJul 30, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K842976

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.