# Medical Devices; Neurological Devices; Classification of the Neuropsychiatric Interpretive Electroencephalograph Assessment Aid
> **Food and Drug Administration** · Final order. · Published 2014-02-18 · Effective 2014-03-20 · 79 FR 9083
## Document
- **Document number:** 2014-03388
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 79 FR 9083
- **CFR reference:** 21 CFR 882
- **Publication date:** 2014-02-18
- **Effective date:** 2014-03-20
- **HHS docket:** Docket No. FDA-2013-M-0042
## Abstract

The Food and Drug Administration (FDA) is classifying the neuropsychiatric interpretive electroencephalograph (EEG) assessment aid into class II (special controls). The Agency is classifying the device into class II (special controls) in order to provide a reasonable assurance of safety and effectiveness of the device.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2014/02/18/2014-03388/medical-devices-neurological-devices-classification-of-the-neuropsychiatric-interpretive)
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