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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Lenses, Soft Contact, Daily Wear
510(k) Number K050717
Device Name PROCLEAR ULTRAVUE TORIC, PROCLEAR ULTRAVUE MULTIFOCAL, PROCLEAR ULTRAVUE 200T MULTIFOCAL TORIC
Applicant
CooperVision, Inc.
711 N. Rd.
Scottsville,,  NY  14546
Applicant Contact BONNIE TSYMBAL
Correspondent
CooperVision, Inc.
711 N. Rd.
Scottsville,,  NY  14546
Correspondent Contact BONNIE TSYMBAL
Regulation Number886.5925
Classification Product Code
LPL  
Date Received03/21/2005
Decision Date 05/13/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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