ClearanceBrief
510(k) K052240 ยท QYX Outpatient Cardiac Telemetry

CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002

ApplicantCardionet, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Oct 19, 2005
ReceivedAug 17, 2005
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K052240

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.