Oklahoma Digital Technologies, Inc.
Country not established
- Devices
- 1
What Oklahoma Digital Technologies, Inc. makes
Oklahoma Digital Technologies, Inc. manufactures the PXI (Personal X-Ray Imager) 512, a portable X-ray imaging device designed for medical diagnostics. This system is intended for capturing high-resolution radiographic images in various clinical settings, including emergency rooms, mobile imaging units, and field deployments.
The PXI (Personal X-Ray Imager) 512 is classified as a Class II medical device under FDA regulations and has undergone the 510(k) clearance process. The company is based in the United States, and its devices are listed in the FDA’s 510(k) registry.
Catalogue
Pxi (Personal X-Ray Imager) 512 Ref K881993
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oklahoma Digital Technologies, Inc. have in the registry?
The registry currently lists 1 device for Oklahoma Digital Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oklahoma Digital Technologies, Inc.'s devices?
Among its 1 most recently registered device, Oklahoma Digital Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Oklahoma Digital Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oklahoma Digital Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oklahoma Digital Technologies, Inc. in the registry?
The most recently registered devices listed for Oklahoma Digital Technologies, Inc. include PXI (PERSONAL X-RAY IMAGER) 512.