FDA 510(k) Application Details - K030884

Device Classification Name	Cleanser, Root Canal   More FDA Info for this Device
510(K) Number	K030884
Device Name	Cleanser, Root Canal
Applicant	ACADENTAL 5830 WOODSON ST. SUITE 5 MISSION, KS 66202 US Other 510(k) Applications for this Company
Contact	CHRISTOPHER CRAIG Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	KJJ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/20/2003
Decision Date	05/27/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review