FDA 510(k) Application Details - K032136

Device Classification Name	Alloy, Metal, Base   More FDA Info for this Device
510(K) Number	K032136
Device Name	Alloy, Metal, Base
Applicant	BEGO U.S.A. 24 ALBION RD. SUITE 103 LINCOLN, RI 02865 US Other 510(k) Applications for this Company
Contact	WILLIAM OREMUS Other 510(k) Applications for this Contact
Regulation Number	872.3710   More FDA Info for this Regulation Number
Classification Product Code	EJH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/11/2003
Decision Date	09/04/2003
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