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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Forceps, Ophthalmic
510(k) Number K811658
Device Name ANIS LENS IMPLANT FORCEPS #2
Applicant
American V. Mueller
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
American V. Mueller
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number886.4350
Classification Product Code
HNR  
Date Received06/12/1981
Decision Date 06/26/1981
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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