FDA 510(k) Application Details - K212969

Device Classification Name	More FDA Info for this Device
510(K) Number	K212969
Device Name	Liposaver
Applicant	LHbiomed Co., Ltd. #806, Medical device Complex Center, 200, Gieopdosi-ro, Jijeong-myeon Wonju-si 26354 KR Other 510(k) Applications for this Company
Contact	Seongsoo Hong Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	QPB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/16/2021
Decision Date	08/07/2024
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