FDA 510(k) Application Details - K220064

Device Classification Name	Light Based Over The Counter Wrinkle Reduction   More FDA Info for this Device
510(K) Number	K220064
Device Name	Light Based Over The Counter Wrinkle Reduction
Applicant	YRS Group Inc 5151 S Procyon St Suite 105 Las Vegas, NV 89118 US Other 510(k) Applications for this Company
Contact	Raphael Arvili 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	01/10/2022
Decision Date	07/22/2022
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