FDA 510(k) Application Details - K023671

Device Classification Name	Varnish, Cavity   More FDA Info for this Device
510(K) Number	K023671
Device Name	Varnish, Cavity
Applicant	CHX TECHNOLOGIES, INC. 4800 DUNDAS ST. WEST SUITE 105 TORONTO, ONTARIO M9A 1B1 CA Other 510(k) Applications for this Company
Contact	ROSS PERRY Other 510(k) Applications for this Contact
Regulation Number	872.3260   More FDA Info for this Regulation Number
Classification Product Code	LBH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/01/2002
Decision Date	11/25/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review