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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name accessories, soft lens products
510(k) Number K014202
Device Name COMPLETE BRAND MULTI-PURPOSE SOLUTION
Original Applicant
ALLERGAN, INC.
2525 dupont dr.
irvine,  CA  92612
Original Contact paul j nowacki
Regulation Number886.5928
Classification Product Code
LPN  
Date Received12/21/2001
Decision Date 02/20/2002
Decision substantially equivalent (SESE)
Regulation Medical Specialty Ophthalmic
510k Review Panel Ophthalmic
summary summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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