FDA 510(k) Application Details - K220831

Device Classification Name	Controller, Foot, Handpiece And Cord   More FDA Info for this Device
510(K) Number	K220831
Device Name	Controller, Foot, Handpiece And Cord
Applicant	Foshan COXO Medical Instrument Co., Ltd. BLDG 4, Dist A, Guangdong New Light Source Industrial Base, South of Luocun Ave, Nanhai Dist Foshan 528226 CN Other 510(k) Applications for this Company
Contact	Yongjian Zheng Other 510(k) Applications for this Contact
Regulation Number	872.4200   More FDA Info for this Regulation Number
Classification Product Code	EBW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/22/2022
Decision Date	09/27/2022
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