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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 K913019
Device Name PDI PARALLEL SIDED POST KIT
Applicant
Precident Corp.
9666 Owensmouth Ave.
Unit "O"
Chatsworth,  CA  91311
Applicant Contact ALLEN M.HANS,P.E.
Correspondent
Precident Corp.
9666 Owensmouth Ave.
Unit "O"
Chatsworth,  CA  91311
Correspondent Contact ALLEN M.HANS,P.E.
Regulation Number872.3810
Classification Product Code
ELR  
Date Received07/09/1991
Decision Date 10/02/1991
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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