FDA 510(k) Applications Submitted by ZVI LADIN, PH.D.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K980537	02/11/1998	ND: YAG ACCESSORY FOR PHOTODERM SYSTEM	ESC MEDICAL SYSTEMS LTD.
K001263	04/19/2000	SHARPLAN LASERS, INC. PULSED CTH:YAG HOLMIUM SURGICAL LASER, MODEL 2040	E S C SHARPLAN
K991628	05/11/1999	MODIFIED LX-20 CO2 LASER SYSTEM FAMILY, LX-20SA	ESC MEDICAL SYSTEMS, INC.
K972028	06/02/1997	DERMASCAN SURGICAL LASER SCANNER	ESC MEDICAL SYSTEMS LTD.
K991935	06/09/1999	EPILIGHT HAIR REMOVAL SYSTEM, PHOTODERM HR SYSTEM	ESC MEDICAL SYSTEMS LTD.
K982119	06/16/1998	DIODE LASER	ESC MEDICAL SYSTEMS LTD.
K972872	08/04/1997	DERMA K LASER SYSTEM	ESC MEDICAL SYSTEMS LTD.
K092328	08/04/2009	MED-SEG, MODEL BTMS 1000	BARTRON MEDICAL IMAGING, INC.
K072331	08/20/2007	RADIANCY MISTRAL DEVICE	RADIANCY (ISRAEL) LTD.
K082423	08/22/2008	NO!NO! SKIN	RADIANCY (ISRAEL) LTD.
K072883	10/09/2007	ICE-SENSE	ARBEL MEDICAL LTD.
K964253	10/24/1996	DERMA 20 LASER SYSTEM	ESC MEDICAL SYSTEMS LTD.
K994014	11/26/1999	ESC INTENSE PULSED LIGHT SYSTEMS: EPILIGHT AND MULTILIGHT	ESC MEDICAL SYSTEMS LTD.
K974536	12/02/1997	PHOTODERM HR SYSTEM	ESC MEDICAL SYSTEMS LTD.
K083620	12/08/2008	SOMNOLYZER 24X7	THE SIESTA GROUP NORTH AMERICA
K123806	12/10/2012	FIBROSCAN	ECHOSENS