# K020903: Docxs B Series Electrodes

- Pathway: 510(k) (Traditional)
- Applicant: Docxs, LLC
- Decided: Sep 26, 2002 after 190 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
Biopotential skin electrodes will be used by the Bio Medical community in both clinical and research applications of the acquisition of all surface biopotentials, standards, and reference, i.e. ElectroencephaloSraph (EEG), Electrocardiograph (ECG), Electromyography (EMG), Electrooculograph (EOG).

Source page: https://510kreport.com/device/K020903
Methodology: https://510kreport.com/methodology