FDA 510(k) Applications Submitted by AMIR WALDMAN, PH.D

FDA 510(k) Number	Submission Date	Device Name	Applicant
K030186	01/21/2003	POLRIS LV	SYNERON MEDICAL LTD.
K050452	02/22/2005	AURORA SR AND SRA APPLICATOR	SYNERON MEDICAL LTD.
K050796	03/29/2005	AURORA DS, DS APPLICATOR	SYNERON MEDICAL LTD.
K031489	05/12/2003	PITANGA	SYNERON MEDICAL LTD.
K121435	05/14/2012	SILKN BLUE	HOME SKINOVATIONS LTD.
K031671	05/29/2003	POLARIS WR	SYNERON MEDICAL LTD.
K031988	06/27/2003	AURORA DS	SYNERON MEDICAL LTD.
K031993	06/27/2003	AURORA SR	SYNERON MEDICAL LTD.
K022266	07/12/2002	AURORA SR	SYNERON MEDICAL LTD.
K041959	07/21/2004	POLARIS DS/COMET	SYNERON MEDICAL LTD.
K041969	07/22/2004	AURORA DS	SYNERON MEDICAL LTD.
K082298	08/12/2008	FLASH N' GO	HOME SKINOVATIONS LTD.
K032514	08/14/2003	AC APPLICATOR, AURORA AC	SYNERON MEDICAL LTD.
K052324	08/25/2005	POLARIS LV, LVA APPLICATOR	SYNERON MEDICAL LTD.
K102461	08/27/2010	FRACTORA	INVASIX LTD.
K072906	10/11/2007	SILK'N	HOME SKINOVATIONS LTD.
K103184	10/29/2010	SILK'N FLASH N GO	HOME SKINOVATIONS LTD.
K033586	11/13/2003	MODIFICATION TO AURORA DS	SYNERON MEDICAL LTD.
K024064	12/09/2002	POLARIS DS	SYNERON MEDICAL LTD.
K053616	12/28/2005	POLARIS WR, ST APPLICATOR	SYNERON MEDICAL LTD.
K110301	02/02/2011	SILK'N FX	HOME SKINOVATIONS LTD.
K120582	02/27/2012	HEATLUX	HOME SKINOVATIONS LTD.
K021149	04/10/2002	AURORA DS	SYNERON MEDICAL LTD.