Applied Neuroscience, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3004577596
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
What Applied Neuroscience, Inc. makes
Applied Neuroscience, Inc. manufactures the NeuroGuide Analysis System, which is a software-based device used for the analysis of electroencephalogram (EEG) data.
The company is based in the United States, and its device is classified as Class II and listed in the FDA 510(k) regulatory registry.
Catalogue
Neuroguide Analysis System Ref K041263
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3004577596
- Address
- 248 176TH TERRACE DR E, REDINGTON SHORES, FL, 33708
Frequently asked questions
How many devices does Applied Neuroscience, Inc. have in the registry?
The registry currently lists 1 device for Applied Neuroscience, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Applied Neuroscience, Inc.'s devices?
Among its 1 most recently registered device, Applied Neuroscience, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Applied Neuroscience, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Applied Neuroscience, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Applied Neuroscience, Inc. in the registry?
The most recently registered devices listed for Applied Neuroscience, Inc. include NEUROGUIDE ANALYSIS SYSTEM.