ClearanceBrief
510(k) K802472 ยท DSI Detector And Alarm, Arrhythmia

BIOMETRIC ERG SYSTEM

ApplicantBiometric Analysis Group, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 26, 1980
ReceivedOct 9, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802472

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.