DEI MODEL 20 EEG— 510(k) K961718

Name: FDA 510(k) clearance K961718
Creator: U.S. Food and Drug Administration
Published: 1996-08-27

Substantially Equivalent

Discovery Engineering Intl., Inc.

FDA 510(k) clearance K961718 for DEI MODEL 20 EEG, Substantially Equivalent on 1996-08-27. Applicant: Discovery Engineering Intl., Inc.. Device class: 2.

Clearance details

Applicant: Discovery Engineering Intl., Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1996-05-02
Decision date: 1996-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Topeka, KS, US

Download summary PDF View on FDA.gov ↗

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