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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Inserter/Remover Contact Lens
510(k) Number K780664
Device Name SOFT LENS REMOVER/INSERTER/MANIPULATOR
Applicant
Dmv Contact Lens Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Dmv Contact Lens Co.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number886.5420
Classification Product Code
KYE  
Date Received04/20/1978
Decision Date 05/17/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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