Cardionet, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1005, CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1004
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cardionet, Inc. Cardiovascular ✕
6 devices
Cleared
Apr 08, 2010
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION
Cardiovascular
170d
Cleared
Dec 05, 2007
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1005
Cardiovascular
85d
Cleared
Nov 14, 2006
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1004
Cardiovascular
21d
Cleared
Apr 25, 2006
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1003
Cardiovascular
154d
Cleared
Oct 19, 2005
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002
Cardiovascular
63d
Cleared
Feb 01, 2002
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1001
Cardiovascular
199d