FDA 510(k) Application Details - K992233

Device Classification Name	Locator, Root Apex   More FDA Info for this Device
510(K) Number	K992233
Device Name	Locator, Root Apex
Applicant	DENT CORP. RESEARCH & DEVELOPMENT 7-11 S.BROADWAY WHITE PLAINS, NY 10601 US Other 510(k) Applications for this Company
Contact	DAVID ALBELDA 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	06/25/1999
Decision Date	11/30/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review