Focal Change
Country not established
- Devices
- 1
What Focal Change makes
Focal Change makes DBA Focal Change Frames.
The device is classified as Class I and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dba Focal Change Frames Ref K923415
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Focal Change have in the registry?
The registry currently lists 1 device for Focal Change. Devices recorded under merged duplicate company entries are counted once.
Which registries list Focal Change's devices?
Among its 1 most recently registered device, Focal Change has devices listed in FDA 510(k) (1 device).
What risk classes do Focal Change's devices fall under?
Among its 1 most recently registered device, the classes recorded for Focal Change's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Focal Change in the registry?
The most recently registered devices listed for Focal Change include DBA FOCAL CHANGE FRAMES.