Xeroradiography
Country not established
- Devices
- 1
What Xeroradiography makes
Xeroradiography manufactures the Xeroradiography 125 System - Modified, which is a diagnostic imaging device.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Xeroradiography 125 System - Modified Ref K761022
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Xeroradiography have in the registry?
The registry currently lists 1 device for Xeroradiography. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xeroradiography's devices?
Among its 1 most recently registered device, Xeroradiography has devices listed in FDA 510(k) (1 device).
What risk classes do Xeroradiography's devices fall under?
Among its 1 most recently registered device, the classes recorded for Xeroradiography's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xeroradiography in the registry?
The most recently registered devices listed for Xeroradiography include XERORADIOGRAPHY 125 SYSTEM - MODIFIED.