510(k) Report

FDA applicant

Epi-Scan Corp.

Russellville, AL1 decision1988–19880 recalls

FDA records 1 decision for Epi-Scan Corp. (Russellville, AL) in 1988: 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 Epi-Scan Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Epi-Scan Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Epi-Scan Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Epi-Scan Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • GZODevice, Galvanic Skin Response Measurement1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K874850Epi-Scan Selective Tissue Conductance MeterEpi-Scan Corp. · 19881cites it

What has FDA decided for it lately?

  • K874850Epi-Scan Selective Tissue Conductance MeterEpi-Scan Corp. · 1988

The one decision as Epi-Scan Corp. →