FDA 510(k) Application Details - K033049

Device Classification Name	Powder, Porcelain   More FDA Info for this Device
510(K) Number	K033049
Device Name	Powder, Porcelain
Applicant	NORITAKE CO., INC. 3050 K STREET, NW, STE 400 WASHINGTON, DC 20007 US Other 510(k) Applications for this Company
Contact	IVAN J WASSERMAN 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	09/29/2003
Decision Date	10/24/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review