# The Electrode Store, Inc.

- Location (FDA's records): Seattle, WA
- FDA decisions: 6 (1995–2009): 6 510(k) clearances
- Product codes: GXY (3), GXZ (2), IKT (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Ives Eeg Solutions, Inc.: 1 (https://510kreport.com/company/ives-eeg-solutions)
- Neurovirtual USA, Inc.: 1 (https://510kreport.com/company/neurovirtual-usa)

## Its most-cited devices
- K022197: Surface Electrode for Electroencephalography (2002), cited by 2

## Recent decisions
- K083758: Sensory Nerve Electrodes-Two Finger Rings, Stimulator Probe Electrodes-Facial, Mono, BI- & Tripolar Nerve Stimulators (Aug 14, 2009)
- K022197: Surface Electrode for Electroencephalography (Aug 13, 2002)
- K020910: Subdermal Needle Electrode for Electroencephalography, Models Pro-E12SAF and Den-12SAF (Jul 19, 2002)
- K020445: The Electrode Store Surface (Cutaneous) Electrode for Emg (May 10, 2002)
- K926094: Protectrode System (Dec 6, 1995)
- K932691: Protectrode Systems Concentric (Nov 16, 1995)

Source page: https://510kreport.com/company/electrode-store