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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name chart, visual acuity
510(k) Number K875237
Device Name OPTEC 1000 DMV VISION TESTER MODIFY
Applicant
STEREO OPTICAL CO., INC.
3539 NORTH KENTON
CHICAGO,  IL  60641
Applicant Contact JOSEPH ANDERA
Correspondent
STEREO OPTICAL CO., INC.
3539 NORTH KENTON
CHICAGO,  IL  60641
Correspondent Contact JOSEPH ANDERA
Regulation Number886.1150
Classification Product Code
HOX  
Date Received12/22/1987
Decision Date 03/17/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
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