Medrad/Technology For People
Country not established
- Devices
- 1
What Medrad/Technology For People makes
The company produces digital subtraction angiography devices, which are used in interventional radiology to visualize blood vessels and guide procedures like stent placement or embolization.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Digital Subtraction Angiography Conven- Ref K830025
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medrad/Technology For People have in the registry?
The registry currently lists 1 device for Medrad/Technology For People. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medrad/Technology For People's devices?
Among its 1 most recently registered device, Medrad/Technology For People has devices listed in FDA 510(k) (1 device).
What risk classes do Medrad/Technology For People's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medrad/Technology For People's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medrad/Technology For People in the registry?
The most recently registered devices listed for Medrad/Technology For People include DIGITAL SUBTRACTION ANGIOGRAPHY CONVEN-.