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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 K884277
Device Name AD POST
Applicant
J. Morita USA, Inc.
9 Mason
Irvine,  CA  92618
Applicant Contact RONALD D NEWMAN
Correspondent
J. Morita USA, Inc.
9 Mason
Irvine,  CA  92618
Correspondent Contact RONALD D NEWMAN
Regulation Number872.3810
Classification Product Code
ELR  
Date Received10/12/1988
Decision Date 12/22/1988
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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