FDA 510(k) Application Details - K230720

Device Classification Name	Over-The-Counter Powered Light Based Laser For Acne   More FDA Info for this Device
510(K) Number	K230720
Device Name	Over-The-Counter Powered Light Based Laser For Acne
Applicant	Light Tree Ventures Europe B.V. Laan van Ypenburg 108, 2497 GC, The Hague, The Netherlands Hague NL Other 510(k) Applications for this Company
Contact	Kim Laurens 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	03/16/2023
Decision Date	07/03/2023
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