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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name cement, dental
510(k) Number K062519
Device Name NEXUS 3
Applicant
KERR CORPORATION
100 BAYVIEW CIRCLE STE 6000
NEWPORT BEACH,  CA  92660
Applicant Contact COLLEEN BOSWELL
Correspondent
KERR CORPORATION
100 BAYVIEW CIRCLE STE 6000
NEWPORT BEACH,  CA  92660
Correspondent Contact COLLEEN BOSWELL
Regulation Number872.3275
Classification Product Code
EMA  
Date Received08/28/2006
Decision Date 10/19/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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