FDA 510(k) Application Details - K183284

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K183284
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	Jeisys Medical Inc. 307,Daeryung Techno Town 8th, Gamasan-ro 96, Geumcheon-Gu Seoul 153-775 KR Other 510(k) Applications for this Company
Contact	Sugun Lee 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	11/26/2018
Decision Date	01/15/2020
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