FDA 510(k) Application Details - K062519

Device Classification Name	Cement, Dental   More FDA Info for this Device
510(K) Number	K062519
Device Name	Cement, Dental
Applicant	KERR CORPORATION 100 BAYVIEW CIRCLE STE 6000 NEWPORT BEACH, CA 92660 US Other 510(k) Applications for this Company
Contact	COLLEEN BOSWELL Other 510(k) Applications for this Contact
Regulation Number	872.3275   More FDA Info for this Regulation Number
Classification Product Code	EMA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/28/2006
Decision Date	10/19/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review