# K190700: Electrodes Pad

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Bestpad Technology Development Co., Ltd.
- Decided: Jun 14, 2019 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: 8 generations back to K903402 (1990). 18 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171381: Adhesive Electrodes, Shenzhen Quality Medical Technology Co.,Ltd (2017) Summary page 4.
- K132998: Wandy Self-Adhesive Electrodes, Wandy Rubber Industrial Co., Ltd. (2013) Summary page 4.

## Most influential descendants
- K221589: Starly pad (2023), 0 descendants of its own

## Indications for use
ELECTRODES PAD is intended to transmit electrical current to patient skin for use with legally marketed electrical stimulation devices, i.e. TENS (Transcutaneous Electrical Nerve Stimulation) and EMS (Electrical Muscular Stimulation). The PAD is for OTC (Over-The-Counter) or Prescription use. The PAD is for adults only.

Source page: https://510kreport.com/device/K190700
Methodology: https://510kreport.com/methodology