Biometrak Corp.
Country not established
- Devices
- 1
What Biometrak Corp. makes
Biometrak Corp. produces the SPECTRAL EEG MONITOR MODEL B500, which is a medical device used for electroencephalography monitoring.
The device is classified as Class II and is listed in the FDA 510(k) registry. Biometrak Corp. is based in the US.
Catalogue
Spectral Eeg Monitor Model B500 Ref K913051
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biometrak Corp. have in the registry?
The registry currently lists 1 device for Biometrak Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biometrak Corp.'s devices?
Among its 1 most recently registered device, Biometrak Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Biometrak Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Biometrak Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biometrak Corp. in the registry?
The most recently registered devices listed for Biometrak Corp. include SPECTRAL EEG MONITOR MODEL B500.