EE1114, 1118, 1121 ELECTRO-ENCEPHALOGRAPH— 510(k) K903004

Name: FDA 510(k) clearance K903004
Creator: U.S. Food and Drug Administration
Published: 1990-11-15

Substantially Equivalent

Teca, Inc.

FDA 510(k) clearance K903004 for EE1114, 1118, 1121 ELECTRO-ENCEPHALOGRAPH, Substantially Equivalent on 1990-11-15. Applicant: Teca, Inc.. Device class: 2.

Clearance details

Applicant: Teca, Inc.
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 1990-07-09
Decision date: 1990-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasantiville, NY, US

Download summary PDF View on FDA.gov ↗

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