Videolabs, Inc.
Country not established
- Devices
- 1
What Videolabs, Inc. makes
Videolabs, Inc. manufactures the MedCam ProPlus, a video camera system with an integrated light source designed for medical imaging applications.
The MedCam ProPlus is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Videolabs, Inc. have in the registry?
The registry currently lists 1 device for Videolabs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Videolabs, Inc.'s devices?
Among its 1 most recently registered device, Videolabs, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Videolabs, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Videolabs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Videolabs, Inc. in the registry?
The most recently registered devices listed for Videolabs, Inc. include VIDEOLABS MEDCAM PROPLUS VIDEO CAMERA AND INTEGRAL LIGHT SOURCE.