ClearanceBrief
510(k) K853669 ยท DSI Detector And Alarm, Arrhythmia

MODEL 43400A REAL-TIME AMBULATORY ECG MONITOR ANAL

ApplicantHewlett-Packard Co., Mcminnville OR, US
DecisionSubstantially Equivalent, Mar 31, 1986
ReceivedSep 3, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853669

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.