FDA 510(k) Application Details - K233114

Device Classification Name	Light Based Over The Counter Wrinkle Reduction   More FDA Info for this Device
510(K) Number	K233114
Device Name	Light Based Over The Counter Wrinkle Reduction
Applicant	Shenzhen Idea Light Limited 3rd Floor, Block B, Shengdelan Industry Park, Longhua District, Shenzhen City, Guangdong Province, China. Shenzhen 518000 CN Other 510(k) Applications for this Company
Contact	Liu Nicole 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	09/27/2023
Decision Date	01/12/2024
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