FDA 510(k) Applications Submitted by CARDIONET, INC
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K012241 |
07/17/2001 |
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1001 |
CARDIONET, INC |
| K052240 |
08/17/2005 |
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002 |
CARDIONET, INC |
| K072558 |
09/11/2007 |
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1005 |
CARDIONET, INC |
| K063222 |
10/24/2006 |
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1004 |
CARDIONET, INC |
| K053263 |
11/22/2005 |
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1003 |
CARDIONET, INC |
| K093288 |
10/20/2009 |
CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION |
CARDIONET, INC |
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