Scandia Corporation
Country not established
- Devices
- 1
What Scandia Corporation makes
Scandia Corporation manufactures the SCANDIA-45 Gamma Camera System, a diagnostic imaging device used for nuclear medicine procedures to capture and display functional images of the body.
The SCANDIA-45 Gamma Camera System is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Scandia-45 Gamma Camera System Ref K101391
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scandia Corporation have in the registry?
The registry currently lists 1 device for Scandia Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scandia Corporation's devices?
Among its 1 most recently registered device, Scandia Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Scandia Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Scandia Corporation's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Scandia Corporation in the registry?
The most recently registered devices listed for Scandia Corporation include SCANDIA-45 GAMMA CAMERA SYSTEM.