FDA 510(k) Application Details - K012673

Device Classification Name	Adhesive, Bracket And Tooth Conditioner, Resin   More FDA Info for this Device
510(K) Number	K012673
Device Name	Adhesive, Bracket And Tooth Conditioner, Resin
Applicant	PRIME DENTAL MANUFACTURING, INC. 3735 WEST BELMONT AVE. CHICAGO, IL 60618 US Other 510(k) Applications for this Company
Contact	ROLANDO MARASIGAN Other 510(k) Applications for this Contact
Regulation Number	872.3750   More FDA Info for this Regulation Number
Classification Product Code	DYH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/14/2001
Decision Date	10/24/2001
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