FDA 510(k) Application Details - K231495

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K231495
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	InMode Ltd. Tabor Building, Shaar Yokneam POB 44 Yokneam Iillit 2069200 IL Other 510(k) Applications for this Company
Contact	Suhair Francis 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	05/23/2023
Decision Date	10/13/2023
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