FDA 510(k) Application Details - K100247

Device Classification Name	Cement, Dental   More FDA Info for this Device
510(K) Number	K100247
Device Name	Cement, Dental
Applicant	DETAX GMBH & CO. KG AMSTEL 320-I AMSTERDAM D-76275 NL Other 510(k) Applications for this Company
Contact	DAGMAR MAESER Other 510(k) Applications for this Contact
Regulation Number	872.3275   More FDA Info for this Regulation Number
Classification Product Code	EMA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/27/2010
Decision Date	07/23/2010
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