FDA 510(k) Application Details - K210129

Device Classification Name	More FDA Info for this Device
510(K) Number	K210129
Device Name	RF Thermal System
Applicant	Luvo Medical Technologies, Inc 125 Fleming Drive Cambridge N1T 2B8 CA Other 510(k) Applications for this Company
Contact	Gregory Berzak Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PBX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/19/2021
Decision Date	07/20/2021
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