FDA 510(k) Application Details - K022020

Device Classification Name	Locator, Root Apex   More FDA Info for this Device
510(K) Number	K022020
Device Name	Locator, Root Apex
Applicant	TOEI ELECTRIC CO., LTD. PO BOX 7007 DEERFIELD, IL 60015 US Other 510(k) Applications for this Company
Contact	DANIEL KAMM Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LQY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	06/20/2002
Decision Date	07/02/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review