FDA applicant

Neurocybernetics

Great Neck, NY1 decision2000–20000 recalls

FDA records 1 decision for Neurocybernetics (Great Neck, NY) in 2000: 1 510(k) clearance. All are in product code HCC (Device, Biofeedback). 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 Neurocybernetics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Neurocybernetics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Neurocybernetics

Which product codes does it file in?

What has FDA decided for it lately?