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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Attachment, Precision, All
510(k) Number K882063
Device Name MAGNE-DENT MAGNET/ZEST RETROFIT KEEPER
Applicant
Zest Anchors, Inc.
8861 Balboa Ave. Suite B
San Diego,  CA  92123
Applicant Contact PAUL ZEST
Correspondent
Zest Anchors, Inc.
8861 Balboa Ave. Suite B
San Diego,  CA  92123
Correspondent Contact PAUL ZEST
Regulation Number872.3165
Classification Product Code
EGG  
Date Received05/16/1988
Decision Date 06/13/1988
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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