FDA 510(k) Application Details - K052130

Device Classification Name	Powder, Porcelain   More FDA Info for this Device
510(K) Number	K052130
Device Name	Powder, Porcelain
Applicant	VIDENT 3150 EAST BIRCH ST. BREA, CA 92821 US Other 510(k) Applications for this Company
Contact	BARBARA J LEWANDOWSKI Other 510(k) Applications for this Contact
Regulation Number	872.6660   More FDA Info for this Regulation Number
Classification Product Code	EIH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/05/2005
Decision Date	08/15/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review