# K072016: Cup Electrodes, Gold, Reusable, Silver, Reusable; Cup Electrodes Silver/Silver Chloride Reusable

- Pathway: 510(k) (Traditional)
- Applicant: Technomed Europe
- Decided: Oct 19, 2007 after 88 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: 2 generations back to K942921 (1995). 3 ancestors in all.
6 later devices descend from it; 4 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061148: Rhythmlink Disc Electrodes, Rhythmlink International, LLC (2006) Summary page 1.

## Most influential descendants
- K192564: Disposable Gold Cup EEG Electrodes (2020), 1 descendant of its own
- K190416: Dome Electrode (2019), 1 descendant of its own
- K261442: Charlotte ACC25 Surface Electrode Array; Charlotte ACC25 Reusable Surface Electrode Array (2026), 0 descendants of its own
- K254183: MR Conditional Cup Electrodes (2026), 0 descendants of its own
- K223605: ControlSeal Electrode (ELSB) (2022), 0 descendants of its own

## Indications for use
The Cup Electrodes are intended for non-invasive use with recording and monitoring equipment, (active and reference), of Electromyography (EMG), Electroencephalograph (EEG) and Evoked Potentials.

Source page: https://510kreport.com/device/K072016
Methodology: https://510kreport.com/methodology