# K231167: Conductive Silicone Rubber Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Guangzhou Xinbo Electronic Co., Ltd.
- Decided: Aug 9, 2023 after 106 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
Conductive silicone rubber electrode are cutaneous electrodes to be used with legally marketed TENS, EMS or NMES devices. The Conductive silicone rubber electrodes are non-sterile reusable conductive garments that are intended to deliver the pulses generated by the electrotherapy stimulator to the body surface with which they are in contact. These body parts can include the upper limb including wrist and hand, elbow or shoulder, lower and upper back, lower limb including hip, knee, leg, ankle and feet, and the back of the neck.

Source page: https://510kreport.com/device/K231167
Methodology: https://510kreport.com/methodology