# K022006: Conductive Gel

- Pathway: 510(k) (Traditional)
- Applicant: The Dezac Group
- Decided: Sep 13, 2002 after 86 days
- Product code: GYB (Media, Electroconductive)
- Device class: 2
- Regulation: 21 CFR 882.1275
- 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 K983964 (1998). 1 ancestor in all.
10 later devices descend from it; 2 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983964: Batch #6060 Conductive Gel, Skylark Device Co., Ltd. (1998) Summary page 2.

## Most influential descendants
- K033052: Conductive Eeg Electrolyte (2003), 9 descendants of its own
- K111717: Electro-Gel (2012), 8 descendants of its own
- K190050: Tech Dots - Adhesive and conductive gel (2019), 6 descendants of its own
- K192606: SAC2 - Electrode Cream (2020), 2 descendants of its own
- K161715: EndyGel (2017), 2 descendants of its own

## Indications for use
The Conductive Gel is intended for use with TENS (transcutaneous electrical nerve stimulators) and EMS (electronic muscle stimulators). The Conductive Gel is used with external electrodes to reduce the impedance of the contact between the electrode surface and the skin.

Source page: https://510kreport.com/device/K022006
Methodology: https://510kreport.com/methodology