TECA 1A96, 1A97 AND 1A98 ELECTROENCEPHALOGRAPHS— 510(k) K890881

Name: FDA 510(k) clearance K890881
Creator: U.S. Food and Drug Administration
Published: 1989-03-23

Substantially Equivalent

Teca, Inc.

FDA 510(k) clearance K890881 for TECA 1A96, 1A97 AND 1A98 ELECTROENCEPHALOGRAPHS, Substantially Equivalent on 1989-03-23. 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: 1989-02-21
Decision date: 1989-03-23
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.