FDA 510(k) Application Details - K020898

Device Classification Name	Alloy, Metal, Base   More FDA Info for this Device
510(K) Number	K020898
Device Name	Alloy, Metal, Base
Applicant	IVOCLAR VIVADENT, INC. 175 PINEVIEW DR. AMHERST, NY 14228 US Other 510(k) Applications for this Company
Contact	ANDERJEET GULATI Other 510(k) Applications for this Contact
Regulation Number	872.3710   More FDA Info for this Regulation Number
Classification Product Code	EJH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/24/2002
Decision Date	03/29/2002
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