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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name target, fusion and stereoscopic
510(k) Number K883471
Device Name VKG 1000, VIDEO KERATOMETER
Applicant
TECHNITEX, INC.
11211 RICHMOND AVE., SUITE
103
HOUSTON,  TX  77082
Applicant Contact RICHARD K SNOOK
Correspondent
TECHNITEX, INC.
11211 RICHMOND AVE., SUITE
103
HOUSTON,  TX  77082
Correspondent Contact RICHARD K SNOOK
Regulation Number886.1880
Classification Product Code
HLP  
Date Received08/16/1988
Decision Date 11/08/1988
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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