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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name burr, corneal, battery-powered
510(k) Number K962989
Device Name AMOILS EPITHELIAL SCRUBBER
Applicant
S. PERCY AMOILS
333 WEST WACKER DR.
SUITE 2600
CHICAGO,  IL  60606
Applicant Contact RICHARD O WOOD, ESQ.
Correspondent
S. PERCY AMOILS
333 WEST WACKER DR.
SUITE 2600
CHICAGO,  IL  60606
Correspondent Contact RICHARD O WOOD, ESQ.
Regulation Number886.4070
Classification Product Code
HOG  
Date Received08/01/1996
Decision Date 01/09/1997
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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