FDA 510(k) Application Details - K123304

Device Classification Name	Material, Tooth Shade, Resin   More FDA Info for this Device
510(K) Number	K123304
Device Name	Material, Tooth Shade, Resin
Applicant	IVOCLAR VIVADENT AG 175 PINEVIEW DR. AMHERST, NY 14228 US Other 510(k) Applications for this Company
Contact	DONNA M HARTNETT Other 510(k) Applications for this Contact
Regulation Number	872.3690   More FDA Info for this Regulation Number
Classification Product Code	EBF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/24/2012
Decision Date	01/24/2013
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review