FDA 510(k) Application Details - K244020

Device Classification Name	Light Based Over The Counter Wrinkle Reduction   More FDA Info for this Device
510(K) Number	K244020
Device Name	Light Based Over The Counter Wrinkle Reduction
Applicant	Shenzhen Qianyu Technology Co., Ltd. Room 601, HanÆs Technology Center. No.9988, Shennan Avenue, Maling Community, Yuehai Street, Nanshan District Shenzhen 518000 CN Other 510(k) Applications for this Company
Contact	Guoyang Li Other 510(k) Applications for this Contact
Regulation Number	878.4810   More FDA Info for this Regulation Number
Classification Product Code	OHS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/27/2024
Decision Date	05/01/2025
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