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U.S. Department of Health and Human Services

510(k) Premarket Notification
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510(k) Number K864679
Device Name DZIDRA GLASS FOR USE IN GENERAL MEDICAL
Applicant
Glen Whitten, Dds
312 W. Pear St.
Lakeland,  FL  33801
Correspondent
Glen Whitten, Dds
312 W. Pear St.
Lakeland,  FL  33801
Date Received12/02/1986
Decision Date 02/25/1987
Decision Substantially Equivalent (SESE)
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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