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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Denture, Plastic, Teeth
510(k) Number K844670
Device Name KORVIN VITA RADIOPAQUE PLASTIC TEETH
Applicant
Credent Co.
1934-38 W. N. Ave.
Chicago,  IL  60622
Applicant Contact HENRY KORVIN
Correspondent
Credent Co.
1934-38 W. N. Ave.
Chicago,  IL  60622
Correspondent Contact HENRY KORVIN
Regulation Number872.3590
Classification Product Code
ELM  
Date Received11/30/1984
Decision Date 04/08/1985
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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