# K172887: XinBo Electrode (Model: Neck Therapy Pro - I, Neck Therapy Pro - II, Neck Therapy Pro - III, Neck Therapy Pro - IV)

- Pathway: 510(k) (Traditional)
- Applicant: Guangzhou Xinbo Electronic Co., Ltd.
- Decided: Apr 19, 2018 after 210 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: 6 generations back to K871222 (1987). 22 ancestors in all.
No later device cites it as a predicate yet.
0 of 23 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K053214: Theraknit Garment Electrode, Neurotron Medical (2005) Summary page 4.
- K151693: Dr-Ho's Foot Pad Electrode, Drtv Asia, Ltd. (2015) Summary page 4.
- K121483: Reusable Cutaneous Electrode, Ampcare, LLC (2012) Summary page 4.

## Indications for use
XinBo Electrodes (Model: Neck Therapy Pro - I; Neck Therapy Pro – II; Neck Therapy Pro - III, Neck Therapy Pro - IV) are cutaneous electrodes to be used with legally marketed TENS stimulating devices for which stimulation of the back of the neck and upper back is appropriate. They will deliver the stimulation signals generated by the stimulator to the back of the neck, upper back and shoulder surface areas with which they are in contact.

Source page: https://510kreport.com/device/K172887
Methodology: https://510kreport.com/methodology