BIOFEEDBACK DEVICES & ACCESSORIES— 510(k) K792115

Name: FDA 510(k) clearance K792115
Creator: U.S. Food and Drug Administration
Published: 1980-03-03

Substantially Equivalent

M.O.E Electronics Research & Prod.

FDA 510(k) clearance K792115 for BIOFEEDBACK DEVICES & ACCESSORIES, Substantially Equivalent on 1980-03-03. Applicant: M.O.E Electronics Research & Prod.. Device class: 2.

Clearance details

Applicant: M.O.E Electronics Research & Prod.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1979-10-10
Decision date: 1980-03-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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