FDA 510(k) Application Details - K220729

Device Classification Name	Over-The-Counter Powered Light Based Laser For Acne   More FDA Info for this Device
510(K) Number	K220729
Device Name	Over-The-Counter Powered Light Based Laser For Acne
Applicant	Luminance Medical Ventures, Inc. 2310 Henderson Avenue #1297 Dallas, TX 75201 US Other 510(k) Applications for this Company
Contact	Troy Stites Other 510(k) Applications for this Contact
Regulation Number	878.4810   More FDA Info for this Regulation Number
Classification Product Code	OLP Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/14/2022
Decision Date	06/09/2022
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