Box, Inc.
Country not established
- Devices
- 1
What Box, Inc. makes
Box, Inc. manufactures the BOX DICOM Viewer, a software application designed for viewing, managing, and sharing digital imaging and communications in medicine (DICOM) files within healthcare settings.
The BOX DICOM Viewer is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
BOX DICOM Viewer Ref K151957
510(k) 510(k)
Frequently asked questions
How many devices does Box, Inc. have in the registry?
The registry currently lists 1 device for Box, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Box, Inc.'s devices?
Among its 1 most recently registered device, Box, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Box, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Box, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Box, Inc. in the registry?
The most recently registered devices listed for Box, Inc. include BOX DICOM Viewer.