510(k) Report

FDA applicant

Galloway Technologies, LLC

Saratoga Springs, UT1 decision2003–20030 recalls

FDA records 1 decision for Galloway Technologies, LLC (Saratoga Springs, UT) in 2003: 1 510(k) clearance. All are in product code GZO (Device, Galvanic Skin Response Measurement). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Galloway Technologies, LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Galloway Technologies, LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Galloway Technologies, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • GZODevice, Galvanic Skin Response Measurement1decision

What has FDA decided for it lately?

  • K023355ASYRAGalloway Technologies, LLC · 2003

The one decision as Galloway Technologies, LLC →