# K974495: Neuroamp Eeg Amplifier

- Pathway: 510(k) (Traditional)
- Applicant: Neurocorp, Ltd.
- Decided: Feb 26, 1998 after 90 days
- Product code: GWQ (Full-Montage Standard Electroencephalograph)
- Device class: 2
- Regulation: 21 CFR 882.1400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The NeuraAmp EEG/EP amplifier is an accessory device of integrated systems used for the recording of brain bio-electrical activity. It intended use is for the amplification of brain bio-electrical signals which are recorded from scalp applied electrodes, and analyzed for brain function evaluation.

Source page: https://510kreport.com/device/K974495
Methodology: https://510kreport.com/methodology