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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Case, Contact Lens
510(k) Number K950869
Device Name JC960 2 IN 1 EYEGLASS/CONTACT LENS CASE
Applicant
Jobar Intl., Inc.
220 N. Inglewood Ave.
Inglewood,  CA  90301
Applicant Contact TIM BAKER
Correspondent
Jobar Intl., Inc.
220 N. Inglewood Ave.
Inglewood,  CA  90301
Correspondent Contact TIM BAKER
Regulation Number886.5928
Classification Product Code
LRX  
Date Received02/27/1995
Decision Date 10/27/1995
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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