FDA 510(k) Application Details - K014142

Device Classification Name	Adhesive, Bracket And Tooth Conditioner, Resin   More FDA Info for this Device
510(K) Number	K014142
Device Name	Adhesive, Bracket And Tooth Conditioner, Resin
Applicant	3M UNITEK 2724 SOUTH PECK RD. MONROVIA, CA 91016 US Other 510(k) Applications for this Company
Contact	L. MARLYN SCHEFF 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	12/17/2001
Decision Date	02/28/2002
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