FDA 510(k) Applications Submitted by IRIDEX CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K992298	07/08/1999	IRIDERM, MODEL APEX 800	IRIDEX CORP.
K982031	06/10/1998	OCULIGHT GL WITH THE DERMATOLOGY HANDPIECE	IRIDEX CORP.
K071687	06/18/2007	FAMILI OF IRIDEX IQ LASER SYSTEMS	IRIDEX CORP.
K020374	02/04/2002	OCULIGHT SL/SLX	IRIDEX CORP.
K020849	03/15/2002	APEX 800 LASER SYSTEM, MODEL APEX 800	IRIDEX CORP.
K022228	07/10/2002	FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES	IRIDEX CORP.
K040209	01/30/2004	IRIS MEDICAL IQ 810 PHOTOCOAGULATOR	IRIDEX CORP.
K050562	03/03/2005	OCULIGHT GL/GLX	IRIDEX CORP.
K060905	04/03/2006	IRIDEX OTOPROBE LONG AND SHORT ANGLES, P/N 14310-1 AND 14320-1	IRIDEX CORP.
K031665	05/29/2003	IRIS MEDICAL OCULIGHT GL/GLX LASER SYSTEMS	IRIDEX CORP.
K062074	07/21/2006	IRIDEX WIRELESS FOOTSWITCH	IRIDEX CORP.
K062369	08/14/2006	IRIDEX OCULIGHT TX	IRIDEX CORP.
K121475	05/18/2012	TXCELL SCANNING LASER DELIVERY SYSTEM	IRIDEX CORP.