Xi Tech
Country not established
- Devices
- 1
What Xi Tech makes
Xi Tech manufactures the XISCAN MODEL 1000, a medical device classified as Class II.
The XISCAN MODEL 1000 is regulated under the FDA 510(k) pathway and is listed in the FDA 510(k) registry. Xi Tech is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Xiscan Model 1000 Ref K852346
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Xi Tech have in the registry?
The registry currently lists 1 device for Xi Tech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xi Tech's devices?
Among its 1 most recently registered device, Xi Tech has devices listed in FDA 510(k) (1 device).
What risk classes do Xi Tech's devices fall under?
Among its 1 most recently registered device, the classes recorded for Xi Tech's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xi Tech in the registry?
The most recently registered devices listed for Xi Tech include XISCAN MODEL 1000.