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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Attachment, Precision, All
510(k) Number K915299
Device Name COGAN CORP KITS OF DENTAL HAND INSTRUMENTS
Applicant
Cogan Corp.
2891 NW Ariel Ter.
Portland,  OR  97210
Applicant Contact GERALD L COGAN
Correspondent
Cogan Corp.
2891 NW Ariel Ter.
Portland,  OR  97210
Correspondent Contact GERALD L COGAN
Regulation Number872.3165
Classification Product Code
EGG  
Date Received11/19/1991
Decision Date 01/31/1992
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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