FDA 510(k) Application Details - K992023

Device Classification Name	Powder, Porcelain   More FDA Info for this Device
510(K) Number	K992023
Device Name	Powder, Porcelain
Applicant	NORITAKE CO., INC. 1050 CONNECTICUT AVENUE, N.W. WASHINGTON, DC 20036-5339 US Other 510(k) Applications for this Company
Contact	MARSHA C WERTZBERGER 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	06/16/1999
Decision Date	09/03/1999
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