EEG BIOFEEDBACK DEVICE— 510(k) K842022

Name: FDA 510(k) clearance K842022
Creator: U.S. Food and Drug Administration
Published: 1984-07-20

Substantially Equivalent

Electronics Research & Production

FDA 510(k) clearance K842022 for EEG BIOFEEDBACK DEVICE, Substantially Equivalent on 1984-07-20. Applicant: Electronics Research & Production. Device class: 2.

Clearance details

Applicant: Electronics Research & Production
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1984-05-18
Decision date: 1984-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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