Livmor
Country not established
- Devices
- 1
What Livmor makes
Livmor manufactures the Halo AF Detection System, a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Halo AF Detection System Ref K201208
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Livmor have in the registry?
The registry currently lists 1 device for Livmor. Devices recorded under merged duplicate company entries are counted once.
Which registries list Livmor's devices?
Among its 1 most recently registered device, Livmor has devices listed in FDA 510(k) (1 device).
What risk classes do Livmor's devices fall under?
Among its 1 most recently registered device, the classes recorded for Livmor's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Livmor in the registry?
The most recently registered devices listed for Livmor include Halo AF Detection System.