# K151033: Philips Self-Adhesive Electrodes

- Pathway: 510(k) (Traditional)
- Applicant: Philips Consumer Lifestyle
- Decided: Jul 28, 2015 after 102 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 K945676 (1995). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130987: Valutrode Neurostimlation Electrodes, Axelgaard Mfg. Co., Ltd. (2013) Summary page 4.

## Indications for use
The Philips Self-Adhesive Electrodes are intended for use with the PulseRelief device for applying Transcutaneous Electrical Nerve Stimulation (TENS) and Electrical Muscle Stimulation (EMS)

Source page: https://510kreport.com/device/K151033
Methodology: https://510kreport.com/methodology