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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 K900777
Device Name ITEM #273 CONTACT LENS CASES
Applicant
Magnivision, Inc.
P.O. Box 817
Miami,  FL  33152
Applicant Contact ROY HIRSCHFELD
Correspondent
Magnivision, Inc.
P.O. Box 817
Miami,  FL  33152
Correspondent Contact ROY HIRSCHFELD
Regulation Number886.5928
Classification Product Code
LRX  
Date Received02/20/1990
Decision Date 03/30/1990
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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