# K241512: Electrode Pad

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Deliduo Medical Technology Co.,Ltd
- Decided: Jan 15, 2025 after 231 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: 9 generations back to K945676 (1995). 25 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K182111: DL Self-adhesive Electrode, Shaoxing DL Healthcare Co., Ltd. (2019) Summary page 5.

## Most influential descendants
- K253237: Elde Medical Electrodes (T5/ 5 cm x 5cm electrode T10/ 5 cm x 10cm electrode) (2026), 0 descendants of its own

## Indications for use
It is is intended to transmit electrical current to patient skin for use with transcutaneous electrical stimulation devices. Some common types of the stimulation devices include, but are not limited to TENS (Transcutaneous Electrical Nerve Stimulation) and EMS (Electrical Muscular Stimulation). The electrode is for OTC (Over-The-Counter) or Prescription use.

Source page: https://510kreport.com/device/K241512
Methodology: https://510kreport.com/methodology