Neurosteer, Inc.
Country not established
- Devices
- 1
What Neurosteer, Inc. makes
Neurosteer, Inc. manufactures the Neurosteer EEG Recorder, a device designed for recording and analyzing electroencephalogram (EEG) signals, likely used in clinical or research settings for neurological monitoring.
The company’s portfolio is regulated under FDA’s Class II device classification and requires 510(k) clearance. The EEG Recorder is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Neurosteer EEG Recorder Ref K221563
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neurosteer, Inc. have in the registry?
The registry currently lists 1 device for Neurosteer, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neurosteer, Inc.'s devices?
Among its 1 most recently registered device, Neurosteer, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neurosteer, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neurosteer, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neurosteer, Inc. in the registry?
The most recently registered devices listed for Neurosteer, Inc. include Neurosteer EEG Recorder.