Capscan Corp.
Country not established
- Devices
- 1
What Capscan Corp. makes
Capscan Corp. manufactures biofeedback devices combining electroencephalography (EEG) and electromyography (EMG) systems for monitoring neural and muscle activity in clinical or research settings.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) premarket notification process. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Capscan Corp. have in the registry?
The registry currently lists 1 device for Capscan Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Capscan Corp.'s devices?
Among its 1 most recently registered device, Capscan Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Capscan Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Capscan Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Capscan Corp. in the registry?
The most recently registered devices listed for Capscan Corp. include BIOFEEDBACK ELECTROENCEPHALOGRAPH/ELECTROMYOGRAPH.