FDA 510(k) Application Details - K203795

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K203795
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	STARmed Co., Ltd. B-dong, 4F&12F, 158, Haneulmaeul-ro, IlsanDong-gu Goyang-si 10355 KR Other 510(k) Applications for this Company
Contact	Jun-Young Jung 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	12/28/2020
Decision Date	04/01/2021
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review