FDA 510(k) Application Details - K220996

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K220996
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	CnC Technologies E1101, Gwang Myeong Technopark, 60, Haan-Ro Gwangmyeong-Si 14322 KR Other 510(k) Applications for this Company
Contact	InSang Choi Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	GEI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/04/2022
Decision Date	02/03/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review