# K021537: Multipurpose Neuroplus Electrode, Model A10005

- Pathway: 510(k) (Traditional)
- Applicant: Vermont Medical, Inc.
- Decided: Mar 3, 2003 after 297 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K172703: Disposable Snap Electrode (2017), 0 descendants of its own

## Indications for use
The Vermed A1 0005 electrode is designed to measure muscle activity from the surface of the skin. The A10005 can be used for Sleep Studies, surface EMG, NCS and EP. The A1 0005 electrode is provided in a NON-STERILE format only, and should be used on the surface of the skin.

Source page: https://510kreport.com/device/K021537
Methodology: https://510kreport.com/methodology