FDA 510(k) Application Details - K000393

Device Classification Name	Activator, Ultraviolet, For Polymerization   More FDA Info for this Device
510(K) Number	K000393
Device Name	Activator, Ultraviolet, For Polymerization
Applicant	NOVA/DA VINCI SYSTEMS, INC. 9885 MESA RIM SUITE 127 SAN DIEGO, CA 92121 US Other 510(k) Applications for this Company
Contact	ALAN A CREAMER 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	02/07/2000
Decision Date	03/27/2000
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