Cardionetics, Ltd.
Country not established
- Devices
- 1
What Cardionetics, Ltd. makes
Cardionetics, Ltd. manufactures the C. NET 2100, which is a Class II medical device.
The company is based in the US, and the C. NET 2100 is listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
C. Net 2100 Ref K010396
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardionetics, Ltd. have in the registry?
The registry currently lists 1 device for Cardionetics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardionetics, Ltd.'s devices?
Among its 1 most recently registered device, Cardionetics, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cardionetics, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cardionetics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardionetics, Ltd. in the registry?
The most recently registered devices listed for Cardionetics, Ltd. include C. NET 2100.