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Cardionet, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K093288CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTIONApril 8, 2010
K072558CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1005December 5, 2007
K063222CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1004November 14, 2006
K053263CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1003April 25, 2006
K052240CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002October 19, 2005
K012241CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1001February 1, 2002
K003707CARDIONET AMBULATORY ECG MONITOR, MODEL CN1000AMay 16, 2001