# K151693: Dr-Ho's Foot Pad Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Drtv Asia, Ltd.
- Decided: Oct 9, 2015 after 108 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: 4 generations back to K040512 (2004). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113321: Tens Back Pain Relief System, Savia Limited (2012) Summary page 4.
- K063660: Otc Tens for Low Back Pain Relief, Model WL-2407, Well-Life Healthcare Limited (2007) Summary page 4.

## Most influential descendants
- K172887: XinBo Electrode (Model: Neck Therapy Pro - I, Neck Therapy Pro - II, Neck Therapy Pro - III, Neck Therapy Pro - IV) (2018), 0 descendants of its own

## Indications for use
The Cutaneous Electrodes, "Dr-Ho's Foot Pad Electrodes", are intended to be used with legally marketed electrical stimulating devices such as transcutaneous electrical nerve stimulators or powered muscle stimulators. The cutaneous electrodes will deliver the stimulation signals generated by the stimulator to the bottom of the feet which they are in contact with.

Source page: https://510kreport.com/device/K151693
Methodology: https://510kreport.com/methodology