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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 K925700
Device Name ZEST ANCHOR ADVANCED GENERATION
Applicant
Zest Anchors, Inc.
2061 Wineridge Pl., Suite 100
Escondido,  CA  92029
Applicant Contact PAUL ZEST
Correspondent
Zest Anchors, Inc.
2061 Wineridge Pl., Suite 100
Escondido,  CA  92029
Correspondent Contact PAUL ZEST
Regulation Number872.3165
Classification Product Code
EGG  
Date Received11/12/1992
Decision Date 04/07/1994
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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