ClearanceBrief
510(k) K053263 ยท DSI Detector And Alarm, Arrhythmia

CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1003

ApplicantCardionet, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Apr 25, 2006
ReceivedNov 22, 2005
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K053263

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.