FDA 510(k) Application Details - K102603

Device Classification Name	Material, Tooth Shade, Resin   More FDA Info for this Device
510(K) Number	K102603
Device Name	Material, Tooth Shade, Resin
Applicant	DMG USA, INC. 5 WHITCOMB AVE. AYER, MA 01432 US Other 510(k) Applications for this Company
Contact	PAMELA PAPINEAU 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	09/10/2010
Decision Date	11/17/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review