FDA 510(k) Application Details - K233518

Device Classification Name	Activator, Ultraviolet, For Polymerization   More FDA Info for this Device
510(K) Number	K233518
Device Name	Activator, Ultraviolet, For Polymerization
Applicant	Handpiece Headquarters 620 S. Placentia Avenue Placentia, CA 92870 US Other 510(k) Applications for this Company
Contact	Frederick Wang 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	11/01/2023
Decision Date	11/02/2023
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	Y
Expedited Review