GEODESIC EEG SYSTEM, MODEL 200— 510(k) K012079

Name: FDA 510(k) clearance K012079
Creator: U.S. Food and Drug Administration
Published: 2001-09-19

Substantially Equivalent

Electrical Geodesics, Incorporated

FDA 510(k) clearance K012079 for GEODESIC EEG SYSTEM, MODEL 200, Substantially Equivalent on 2001-09-19. Applicant: Electrical Geodesics, Incorporated. Device class: 2.

Clearance details

Applicant: Electrical Geodesics, Incorporated
Product code: Code GWQ
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 2001-07-03
Decision date: 2001-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Phoenix, AZ, US

Download summary PDF View on FDA.gov ↗

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