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MODIFIED BRAIN ATLAS III

K854362 Class II Traditional
Decision Date
1986-04-22
Sponsor / Applicant
Bio-Logic Systems Corp.

Technical Specification

510(k) Submission ID K854362
Product Code GWE
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.1890
Decision Date 1986-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFIED BRAIN ATLAS III received FDA 510(k) clearance under submission number K854362, 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 1986-04-22.

Classification & Regulation

This clearance is catalogued under FDA product code GWE and 21 CFR 882.1890, within the Neurology review panel as a Class II device.