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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Post, Root Canal
510(k) Number K812092
Device Name BETA POST
Applicant
Paul B. Heller, D.M.D.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Paul B. Heller, D.M.D.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number872.3810
Classification Product Code
ELR  
Date Received07/23/1981
Decision Date 08/20/1981
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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