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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name refractometer, ophthalmic
510(k) Number K771914
Device Name SUBJECTIVE REFRACTOR, MOSEL SR-111
Applicant
AMERICAN OPTICAL CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
AMERICAN OPTICAL CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number886.1760
Classification Product Code
HKO  
Date Received10/12/1977
Decision Date 11/09/1977
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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