Wavestate, Inc.
Country not established
- Devices
- 1
What Wavestate, Inc. makes
Wavestate, Inc. makes the WAVESTATE NEUROMONITOR, a device used for monitoring neurological activity.
The WAVESTATE NEUROMONITOR is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Wavestate Neuromonitor Ref K092625
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wavestate, Inc. have in the registry?
The registry currently lists 1 device for Wavestate, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wavestate, Inc.'s devices?
Among its 1 most recently registered device, Wavestate, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Wavestate, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wavestate, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wavestate, Inc. in the registry?
The most recently registered devices listed for Wavestate, Inc. include WAVESTATE NEUROMONITOR.