FDA 510(k) Application Details - K100150

Device Classification Name	Powder, Porcelain   More FDA Info for this Device
510(K) Number	K100150
Device Name	Powder, Porcelain
Applicant	BIODENTA SWISS AG TRAMSTRASSE 16 BERNECK 9442 CH Other 510(k) Applications for this Company
Contact	DAVID EILER 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	01/19/2010
Decision Date	05/25/2010
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review