FDA 510(k) Application Details - K981620

Device Classification Name	Resin, Root Canal Filling   More FDA Info for this Device
510(K) Number	K981620
Device Name	Resin, Root Canal Filling
Applicant	DENTSPLY INTL. 570 WEST COLLEGE AVE. YORK, PA 17405-0872 US Other 510(k) Applications for this Company
Contact	JEFFERY P LEHN Other 510(k) Applications for this Contact
Regulation Number	872.3820   More FDA Info for this Regulation Number
Classification Product Code	KIF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/06/1998
Decision Date	07/31/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review