Scanrite Systems
Country not established
- Devices
- 1
What Scanrite Systems makes
Scanrite Systems manufactures the SCANRITE DFS, a device designed for digital fluoroscopy imaging used in medical diagnostics. This system enables real-time X-ray imaging to visualize internal structures, supporting procedures such as orthopedic assessments, vascular studies, and interventional radiology.
The SCANRITE DFS is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Scanrite Dfs Ref K970850
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scanrite Systems have in the registry?
The registry currently lists 1 device for Scanrite Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scanrite Systems's devices?
Among its 1 most recently registered device, Scanrite Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Scanrite Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Scanrite Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scanrite Systems in the registry?
The most recently registered devices listed for Scanrite Systems include SCANRITE DFS.