# K043009: Brainet Kit

- Pathway: 510(k) (Traditional)
- Applicant: Jordan Neuroscience, Inc.
- Decided: Jan 12, 2005 after 72 days
- Product code: GXY (Electrode, Cutaneous)
- Device class: 2
- Regulation: 21 CFR 882.1320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K780045 (1978). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K780045: Electrode Cap, Electro-Cap Intl., Inc. (1978) Summary page 1.
- (no number) AMBU Disposable Cup Electrode: named in the summary without a submission number

## Most influential descendants
- K191225: EEG Electrode Template (2019), 0 descendants of its own

## Indications for use
The BraiNet® Kit contents are placed on the scalp to support electroencephalograph (EEG) electrode placement.

Source page: https://510kreport.com/device/K043009
Methodology: https://510kreport.com/methodology