ClearanceBrief
510(k) K811581 ยท DSI Detector And Alarm, Arrhythmia

ARRHYTHMIA FUNCTION BLOCK

ApplicantHoneywell, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 13, 1981
ReceivedJun 5, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K811581

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.