FDA 510(k) Application Details - K992728

Device Classification Name	Activator, Ultraviolet, For Polymerization   More FDA Info for this Device
510(K) Number	K992728
Device Name	Activator, Ultraviolet, For Polymerization
Applicant	SPRING HEALTH PRODUCTS, INC. 705 GENERAL WASHINGTON AVE. #701 NORRISTOWN, PA 19403 US Other 510(k) Applications for this Company
Contact	NATHANIEL H LIEB Other 510(k) Applications for this Contact
Regulation Number	872.6070   More FDA Info for this Regulation Number
Classification Product Code	EBZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/13/1999
Decision Date	09/29/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	DE - Dental
Review Advisory Committee	DE - Dental
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review