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BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM

K973883 Class II Traditional
Decision Date
1998-03-05
Sponsor / Applicant
Bio-Logic Systems Corp.

Technical Specification

510(k) Submission ID K973883
Product Code GWQ
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1400
Decision Date 1998-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIO-LOGIC CEEGRAPH 128-CHANNEL RECORDING SYSTEM received FDA 510(k) clearance under submission number K973883, sponsored by Bio-Logic Systems Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1998-03-05.

Classification & Regulation

This clearance is catalogued under FDA product code GWQ and 21 CFR 882.1400, within the Neurology review panel as a Class II device.