FDA 510(k) Applications Submitted by Sam Wade

FDA 510(k) Number	Submission Date	Device Name	Applicant
K140122	01/16/2014	CANDELA GENTLEMAX FAMILY OF LASER SYSTEM	CANDELA CORP.
K120510	02/21/2012	TRANSCEND	SYNERON MEDICAL LTD.
K140732	03/24/2014	CANDELA GENTLELASE FAMILY OF LASER SYSTEMS	CANDELA CORP.
K180993	04/16/2018	Beacon Advanced CO2 Laser System	OmniGuide, Inc
K122579	08/23/2012	VELASHAPE	SYNERON MEDICAL LTD.
K112715	09/19/2011	CANDELA GENTLEMAX FAMILY OF LASERS	CANDELA CORP.
K133283	10/25/2013	CANDELA GENTLEMAX FAMILY OF LASER SYSTEMS	CANDELA CORP.
K183199	11/19/2018	TRIO Handpiece	OmniGuide, Inc.
K023543	10/22/2002	EVLT KIT AND D15PLUS AND D30PLUS DIODE	DIOMED, INC.
K974300	11/17/1997	TELEMED SYSTEMS RETRIEVAL BASKET	TELEMED SYSTEMS, INC.
K974312	11/17/1997	REUSABLE BIOPSY FORCEPS OVAL CUP, REUSABLE BIOSY FORCEPS OVAL CUP W/NEEDLE, REUSABLE BIOPSY FORCEPS SERRATED CUP, REUSAR	TELEMED SYSTEMS, INC.