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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Resin, Root Canal Filling
510(k) Number K810923
Device Name LEE ENDOFILL, ROOT CANAL FILLING RESIN
Applicant
Lee Pharmaceuticals
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Lee Pharmaceuticals
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number872.3820
Classification Product Code
KIF  
Date Received04/06/1981
Decision Date 04/21/1981
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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