FDA 510(k) Applications Submitted by TOPCON CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K082364	08/18/2008	IMAGENET PROFESSIONAL PC SOFTWARE SYSTEM OR IMAGENET PROFESSIONAL, OR IMAGENET PRO, OR DIGITAL IMAGING SOFTWARE FOR	TOPCON CORP.
K041367	05/24/2004	TOPCON MODEL TRC-NW200 NON-MYDRIATIC RETINAL CAMERA	TOPCON CORP.
K063388	11/08/2006	TOPCON 3D OCT-1000 OPTICAL COHERENCE TOMOGRAPHY SYSTEM	TOPCON CORP.
K130289	02/05/2013	TRC-NW8 NON-MYDRIATIC RETINAL CAMERA	TOPCON CORP.
K141325	05/20/2014	TRC-NW8F PLUS NON-MYDRIATIC RETINAL CAMERA	TOPCON CORP.
K133667	11/29/2013	SLIT LAMP SL-D701	TOPCON CORP.
K090115	01/21/2009	RETINA CAMERA TRC-NW7SF MARK II	TOPCON CORP.
K100207	01/25/2010	NON-MYDRIATIC RETINAL CAMERA, MODEL TRC-NW8F	TOPCON CORP.
K092470	08/12/2009	OPTICAL COHERENCE TOMOGRAPHY 3D OCT-2000	TOPCON CORP.