FDA applicant

Phazx Systems, Inc.

Boulder, CO1 decision1999–19990 recalls

FDA records 1 decision for Phazx Systems, Inc. (Boulder, CO) in 1999: 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 Phazx Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Phazx Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Phazx Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?