Company ยท US
Cardionet, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2010. Name variants (Inc, Corp, punctuation) are merged.
7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Apr 8, 2010 | K093288 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION Cardionet, Inc. | QYX |
| Dec 5, 2007 | K072558 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1005 Cardionet, Inc. | QYX |
| Nov 14, 2006 | K063222 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1004 Cardionet, Inc. | QYX |
| Apr 25, 2006 | K053263 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1003 Cardionet, Inc. | DSI |
| Oct 19, 2005 | K052240 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002 Cardionet, Inc. | QYX |
| Feb 1, 2002 | K012241 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1001 Cardionet, Inc. | DSI |
| May 16, 2001 | K003707 | CARDIONET AMBULATORY ECG MONITOR, MODEL CN1000A Cardionet | MWJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||