Artronics
Country not established
- Devices
- 1
What Artronics makes
Artronics manufactures the NeuroReader, a medical device designed for neurological assessments and monitoring. This device is intended for use in clinical settings to evaluate brain activity and provide diagnostic insights, likely supporting conditions related to epilepsy or other neurological disorders.
The NeuroReader is classified as a Class II device under FDA regulations and has undergone 510(k) clearance. The company is based in the United States, where its products are registered and authorised for commercial distribution.
Catalogue
Neuroreader Ref K950986
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Artronics have in the registry?
The registry currently lists 1 device for Artronics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Artronics's devices?
Among its 1 most recently registered device, Artronics has devices listed in FDA 510(k) (1 device).
What risk classes do Artronics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Artronics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Artronics in the registry?
The most recently registered devices listed for Artronics include NEUROREADER.