Cardionet, LLC
Country not established FDA establishment FEI 3008773647
- Devices
- 7
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- 510(k) 510(k)
- 510(k) 510(k)
- 510(k) 510(k)
- 510(k) 510(k)
Cardionet Ambulatory Ecg Monitor, Model CN1000A Ref K003707
510(k) 510(k)- 510(k) 510(k)
- 510(k) 510(k)
Company details
- FDA FEI number
- 3008773647
- Address
- 5750 S. 40th St Suite 5, Phoenix, AZ, 85040
Frequently asked questions
How many devices does CARDIONET, LLC have in the registry?
The registry currently lists 7 devices for CARDIONET, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list CARDIONET, LLC's devices?
Among its 7 most recently registered devices, CARDIONET, LLC has devices listed in FDA 510(k) (7 devices).
What risk classes do CARDIONET, LLC's devices fall under?
Among its 7 most recently registered devices, the classes recorded for CARDIONET, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CARDIONET, LLC in the registry?
The most recently registered devices listed for CARDIONET, LLC include CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1004, CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1003, CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL CN1001 and CARDIONET AMBULATORY ECG MONITOR WITH ARRHYTHMIA DETECTION, MODEL 1002.