ClearanceBrief
510(k) K780343 ยท DSI Detector And Alarm, Arrhythmia

ARRHYTHMIA TREND ENHANCEMENT

ApplicantAmerican Optical Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 18, 1978
ReceivedMar 2, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780343

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.