# K050788: Everlife

- Pathway: 510(k) (Traditional)
- Applicant: Everlife Medical Instrument Co., Ltd.
- Decided: May 13, 2005 after 46 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: 1 generation back to K022917 (2003). 1 ancestor in all.
22 later devices descend from it; 1 cites it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022917: Home Care Various Models of Self-Adhesive Electrodes, Home Care Technology Co., Ltd. (2003) Summary page 1.

## Most influential descendants
- K062675: Gemore Reuseable Self Adhesive Electrode, Models Wire Series, Snap Series and Double Side Series (2007), 21 descendants of its own
- K083302: Lifecare Electrodes (2009), 14 descendants of its own
- K130987: Valutrode Neurostimlation Electrodes (2013), 10 descendants of its own
- K150971: Zekang Self-adhesive Electrode (2015), 5 descendants of its own
- K082065: Well Life Self Adhesive Electrode / Models: CM, FA, PU and SP (2009), 5 descendants of its own

## Indications for use
Intended to be applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.

Source page: https://510kreport.com/device/K050788
Methodology: https://510kreport.com/methodology