FDA 510(k) Application Details - K961735

Device Classification Name	Activator, Ultraviolet, For Polymerization   More FDA Info for this Device
510(K) Number	K961735
Device Name	Activator, Ultraviolet, For Polymerization
Applicant	SATELEC 70 WALNUT ST. WELLESLEY, MA 02481 US Other 510(k) Applications for this Company
Contact	JACKIE MASSE 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	05/03/1996
Decision Date	07/31/1996
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