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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Frame, Spectacle
510(k) Number K930331
Device Name SPECTACLE FRAME
Applicant
Australian Optical Co., Inc.
1775 Universal Ave.
Suite 1620
Kansas City,  MO  64120
Applicant Contact DEBRA L ALDRIDGE
Correspondent
Australian Optical Co., Inc.
1775 Universal Ave.
Suite 1620
Kansas City,  MO  64120
Correspondent Contact DEBRA L ALDRIDGE
Regulation Number886.5842
Classification Product Code
HQZ  
Date Received01/22/1993
Decision Date 12/08/1993
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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