FDA 510(k) Application Details - K972355

Device Classification Name	Activator, Ultraviolet, For Polymerization   More FDA Info for this Device
510(K) Number	K972355
Device Name	Activator, Ultraviolet, For Polymerization
Applicant	3M COMPANY 3M CENTER BLDG. 275-3SE-08 ST. PAUL, MN 55144-1000 US Other 510(k) Applications for this Company
Contact	LISA A WEIK 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	06/25/1997
Decision Date	08/29/1997
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