Scanditronix Wellhofer North America
Country not established
- Devices
- 1
What Scanditronix Wellhofer North America makes
Scanditronix Wellhofer North America manufactures the DOSE 1, a device designed for precise radiation dose measurement in medical imaging procedures.
The DOSE 1 is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Dose 1 Ref K000209
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scanditronix Wellhofer North America have in the registry?
The registry currently lists 1 device for Scanditronix Wellhofer North America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scanditronix Wellhofer North America's devices?
Among its 1 most recently registered device, Scanditronix Wellhofer North America has devices listed in FDA 510(k) (1 device).
What risk classes do Scanditronix Wellhofer North America's devices fall under?
Among its 1 most recently registered device, the classes recorded for Scanditronix Wellhofer North America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scanditronix Wellhofer North America in the registry?
The most recently registered devices listed for Scanditronix Wellhofer North America include DOSE 1.