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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Implant, Endosseous, Root-Form
510(k) Number K902433
Device Name DIA ANATOMIC ABUTMENT
Applicant
Dental Imaging Assoc., Inc.
3838 Carson St. #102
Torrance,  CA  90503
Applicant Contact PRESTON, D.D.S.
Correspondent
Dental Imaging Assoc., Inc.
3838 Carson St. #102
Torrance,  CA  90503
Correspondent Contact PRESTON, D.D.S.
Regulation Number872.3640
Classification Product Code
DZE  
Date Received05/31/1990
Decision Date 01/17/1992
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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