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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Carboxymethylcellulose Sodium Or Polyvinyl Methylether Maleic Acid Calcium-Sodium
510(k) Number K872225
Device Name SUPER POLI-GRIP & WERNET'S DENTURE ADHES. POWDER
Applicant
Block Drug Company, Inc.
257 Cornelison Ave.
Jersey City,  NJ  07302
Applicant Contact HOWARD FEINMAN
Correspondent
Block Drug Company, Inc.
257 Cornelison Ave.
Jersey City,  NJ  07302
Correspondent Contact HOWARD FEINMAN
Regulation Number872.3490
Classification Product Code
KOT  
Date Received06/09/1987
Decision Date 06/30/1987
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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