FDA 510(k) Application Details - K960104

Device Classification Name	Alloy, Gold-Based Noble Metal   More FDA Info for this Device
510(K) Number	K960104
Device Name	Alloy, Gold-Based Noble Metal
Applicant	DEGUSSA CORP. 3950 SOUTH CLINTON AVE. SOUTH PLAINFIELD, NJ 07080 US Other 510(k) Applications for this Company
Contact	HOLGER MEINICKE Other 510(k) Applications for this Contact
Regulation Number	872.3060   More FDA Info for this Regulation Number
Classification Product Code	EJT Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/11/1996
Decision Date	02/06/1996
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	RA - Radiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review