# K171414: qEEG-Pro

- Pathway: 510(k) (Traditional)
- Applicant: Brainmaster Technologies, Inc.
- Decided: Jul 1, 2018 after 412 days
- Product code: OLU (Normalizing Quantitative Electroencephalograph Software)
- 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: 3 generations back to K801604 (1980). 16 ancestors in all.
4 later devices descend from it; 3 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041263: Neuroguide Analysis System, Applied Neuroscience, Inc. (2004) Summary page 4.

## Most influential descendants
- K202588: BNA Platform (2020), 1 descendant of its own
- K253015: Cognitive Function Neuroimaging (cfNI) Software (1.0.0) (2026), 0 descendants of its own
- K251726: SignalNED System (Model RE) (2025), 0 descendants of its own
- K222838: iSyncBrain©-C (2023), 0 descendants of its own

## Indications for use
The qEEG-Pro System is to be used by qualified medical or qualified clinical professionals for the statistical evaluation of the human electroencephalogram (EEG).

Source page: https://510kreport.com/device/K171414
Methodology: https://510kreport.com/methodology