VEEGix EEG System— 510(k) K240593

Name: FDA 510(k) clearance K240593
Creator: U.S. Food and Drug Administration
Published: 2024-08-23

Substantially Equivalent

NeuroServo, Inc.

FDA 510(k) clearance K240593 for VEEGix EEG System, Substantially Equivalent on 2024-08-23. Applicant: NeuroServo, Inc.. Device class: 2.

Clearance details

Applicant: NeuroServo, Inc.
Product code: Code OLT
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 2024-03-01
Decision date: 2024-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montreal, CA

Download summary PDF View on FDA.gov ↗

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K220254 — Neuron-Spectrum-AM with Neuron-Spectrum.NET Software2022-11-30

Adverse events under product code OLT

product code OLT

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.