FDA 510(k) Application Details - K143040

Device Classification Name	More FDA Info for this Device
510(K) Number	K143040
Device Name	Exilis XP
Applicant	BTL INDUSTRIES INC 47 Loring Drive Framingham, MA 01702 US Other 510(k) Applications for this Company
Contact	Jan Zarsky Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	PBX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/22/2014
Decision Date	01/15/2015
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