FDA 510(k) Application Details - K143741

Device Classification Name	More FDA Info for this Device
510(K) Number	K143741
Device Name	Lipofina Laser System
Applicant	YOLO MEDICAL, INC. 1959 152nd STREET Suite 245 Carpenteria BC V4A 9E3 CA Other 510(k) Applications for this Company
Contact	Robert J Krznaric Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OLI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/31/2014
Decision Date	04/24/2015
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