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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Material, Impression
510(k) Number K895901
Device Name VITA CEREC SET AND VITA CEREC BLOCS
Applicant
Vident
5130 Commerce Dr.
Baldwin Park,  CA  91706
Applicant Contact RAY E MORROW
Correspondent
Vident
5130 Commerce Dr.
Baldwin Park,  CA  91706
Correspondent Contact RAY E MORROW
Regulation Number872.3660
Classification Product Code
ELW  
Date Received10/06/1989
Decision Date 01/17/1992
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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