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GED (GRADUATED ELECTRONIC DECELERATOR

K911820 Class II Traditional
Decision Date
1994-12-05
Sponsor / Applicant
Behavior Research Institute, Inc.

Technical Specification

510(k) Submission ID K911820
Product Code HCB
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5235
Decision Date 1994-12-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GED (GRADUATED ELECTRONIC DECELERATOR received FDA 510(k) clearance under submission number K911820, sponsored by Behavior Research Institute, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 1994-12-05.

Classification & Regulation

This clearance is catalogued under FDA product code HCB and 21 CFR 882.5235, within the Neurology review panel as a Class II device.