FDA 510(k) Application Details - K172273

Device Classification Name	Light, Ultraviolet, Dermatological   More FDA Info for this Device
510(K) Number	K172273
Device Name	Light, Ultraviolet, Dermatological
Applicant	Chongqing Peninsula Medical Technology Co., Ltd. No.2-4, 2F Block I, Ke Yuan 4th Road, Jiulongpo District Chongqing 400041 CN Other 510(k) Applications for this Company
Contact	Zhang Sudi Other 510(k) Applications for this Contact
Regulation Number	878.4630   More FDA Info for this Regulation Number
Classification Product Code	FTC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/28/2017
Decision Date	07/30/2018
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