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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Adhesive, Denture, Carboxymethylcellulose Sodium (40-100&)
510(k) Number K901882
Device Name URESIL ENDOSCOPIC LASER OVERTUBE
Applicant
Uresil Corp.
5418 W. Touhy Ave.
Skokie,  IL  60077
Applicant Contact M GOLDBERG,MD
Correspondent
Uresil Corp.
5418 W. Touhy Ave.
Skokie,  IL  60077
Correspondent Contact M GOLDBERG,MD
Regulation Number872.3410
Classification Product Code
KOQ  
Date Received04/26/1990
Decision Date 07/27/1990
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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