FDA applicant

Neurometrics

Mchenry, IL3 decisions1980–19860 recalls

FDA records 3 decisions for Neurometrics (Mchenry, IL) from 1980 to 1986: 3 510(k) clearances. Most are in product codes GWF (Stimulator, Electrical, Evoked Response) and GWS (Analyzer, Spectrum, Electroencephalogram Signal). 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 Neurometrics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Neurometrics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Neurometrics

Which product codes does it file in?

What has FDA decided for it lately?