510(k) Report

FDA applicant

Bio-Signal Group Corporation

Brooklyn, NY1 decision2012–20120 recalls

FDA records 1 decision for Bio-Signal Group Corporation (Brooklyn, NY) in 2012: 1 510(k) clearance. All are in product code GWQ (Full-Montage Standard Electroencephalograph). 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 Bio-Signal Group Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2012: 1
2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Bio-Signal Group Corporation by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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