Cardionet, Inc.
Cardionet, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 8, 2010.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K093288 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION | April 8, 2010 |
| K072558 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1005 | December 5, 2007 |
| K063222 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1004 | November 14, 2006 |
| K053263 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1003 | April 25, 2006 |
| K052240 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002 | October 19, 2005 |
| K012241 | CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1001 | February 1, 2002 |
| K003707 | CARDIONET AMBULATORY ECG MONITOR, MODEL CN1000A | May 16, 2001 |