Digital Body Systems, Inc.
Country not established
- Devices
- 1
What Digital Body Systems, Inc. makes
Digital Body Systems, Inc. manufactures The HandScan System, a Class I medical device designed for hand imaging and analysis, likely used in diagnostic or monitoring applications.
The HandScan System is regulated under FDA 510(k) clearance as a Class I device and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
The Handscan System Ref K893455
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Digital Body Systems, Inc. have in the registry?
The registry currently lists 1 device for Digital Body Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Digital Body Systems, Inc.'s devices?
Among its 1 most recently registered device, Digital Body Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Digital Body Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Digital Body Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Digital Body Systems, Inc. in the registry?
The most recently registered devices listed for Digital Body Systems, Inc. include THE HANDSCAN SYSTEM.