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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Clamp, Eyelid, Ophthalmic
510(k) Number K831285
Device Name SURGICAL/LID MARGIN COVER & EYELASH-
Applicant
Richard R. Anthony, M.D.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Richard R. Anthony, M.D.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number886.4350
Classification Product Code
HOD  
Date Received04/20/1983
Decision Date 06/03/1983
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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