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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name nystagmograph
510(k) Number K871466
Device Name VESTIBULAR AUTOROTATION TEST
Applicant
WESTERN SYSTEMS RESEARCH, INC.
2265 WESTWOOD BLVD., STE 545
LOS ANGELES,  CA  90064
Applicant Contact LINDA L DAVIS
Correspondent
WESTERN SYSTEMS RESEARCH, INC.
2265 WESTWOOD BLVD., STE 545
LOS ANGELES,  CA  90064
Correspondent Contact LINDA L DAVIS
Regulation Number882.1460
Classification Product Code
GWN  
Date Received04/14/1987
Decision Date 07/24/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Neurology
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
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