NeuroServo, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What NeuroServo, Inc. makes
NeuroServo, Inc. manufactures the VEEGix EEG System, a device designed for continuous electroencephalography monitoring to capture and analyze brain wave activity in clinical settings.
The VEEGix EEG System is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
VEEGix EEG System Ref K240593
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does NeuroServo, Inc. have in the registry?
The registry currently lists 1 device for NeuroServo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list NeuroServo, Inc.'s devices?
Among its 1 most recently registered device, NeuroServo, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do NeuroServo, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for NeuroServo, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from NeuroServo, Inc. in the registry?
The most recently registered devices listed for NeuroServo, Inc. include VEEGix EEG System.