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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Lens, Contact (Polymethylmethacrylate)
510(k) Number K843342
Device Name LENSKEEPER LENS CARRYING CASE
Applicant
Allergan Pharmaceuticals, Inc.
2525 Dupont Dr.
Irvine,  CA  92612
Applicant Contact MARVIN J GARRETT
Correspondent
Allergan Pharmaceuticals, Inc.
2525 Dupont Dr.
Irvine,  CA  92612
Correspondent Contact MARVIN J GARRETT
Classification Product Code
HPX  
Date Received08/27/1984
Decision Date 11/19/1984
Decision Substantially Equivalent (SESE)
510k Review Panel Ophthalmic
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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