FDA 510(k) Application Details - K210567

Device Classification Name	Instrument, Ultrasonic Surgical   More FDA Info for this Device
510(K) Number	K210567
Device Name	Instrument, Ultrasonic Surgical
Applicant	Miconvey Technologies Co., Ltd. No.16 Fangzheng Avenue, Beibei District Chongqing 400714 CN Other 510(k) Applications for this Company
Contact	Kang Li Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LFL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/26/2021
Decision Date	09/30/2022
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review