# K173460: NeuroEEG

- Pathway: 510(k) (Traditional)
- Applicant: Memory MD, Inc.
- Decided: Feb 16, 2018 after 101 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
Longest line of descent: 2 generations back to K941551 (1995). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150498: Discovery 24, Brainmaster Technologies, Inc. (2016) Summary page 4.

## Indications for use
NeuroEEG is intended for prescription use to acquire, record, transmit, and display electrical brain activity of patients of all ages.

Source page: https://510kreport.com/device/K173460
Methodology: https://510kreport.com/methodology