Philips France Commercial
FranceFDA applicant, unverified
- Devices
- 1
What Philips France Commercial makes
Philips France Commercial manufactures the Cardiologs Holter Platform, a device used for continuous ambulatory electrocardiographic monitoring to record heart rhythms over extended periods.
The Cardiologs Holter Platform is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Cardiologs Holter Platform Ref K250569
Regimes: CE MDR 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Philips France Commercial have in the registry?
The registry currently lists 1 device for Philips France Commercial. Devices recorded under merged duplicate company entries are counted once.
Which registries list Philips France Commercial's devices?
Among its 1 most recently registered device, Philips France Commercial has devices listed in FDA 510(k) (1 device).
What risk classes do Philips France Commercial's devices fall under?
Among its 1 most recently registered device, the classes recorded for Philips France Commercial's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Philips France Commercial in the registry?
The most recently registered devices listed for Philips France Commercial include Cardiologs Holter Platform.