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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Agent, Tooth Bonding, Resin
510(k) Number K990040
Device Name CLEARFIL SE BOND
Applicant
Kuraray Co.
200 Park Ave.
New York,  NY  10166
Applicant Contact KOJI FUJITA
Correspondent
Kuraray Co.
200 Park Ave.
New York,  NY  10166
Correspondent Contact KOJI FUJITA
Regulation Number872.3200
Classification Product Code
KLE  
Date Received01/06/1999
Decision Date 02/04/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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