FDA 510(k) Applications Submitted by TOPCON CORPORATION

FDA 510(k) Number Submission Date Device Name Applicant
K161509 06/01/2016 3D OCT-1 Maestro Topcon Corporation
K173119 09/29/2017 DRI OCT Triton Topcon Corporation
K170164 01/18/2017 3D OCT-1 Maestro Topcon Corporation
K171370 05/10/2017 IMAGEnet 6 Ophthalmic Data System Topcon Corporation
K141481 06/04/2014 TRC-NW400 NON-MYDRIATIC RETINAL CAMERA TOPCON CORPORATION
K161972 07/18/2016 Slit Lamp SL-D301 TOPCON CORPORATION
K142417 08/28/2014 SP-1PSpecular Microscope TOPCON CORPORATION
K221111 04/15/2022 Non-Mydriatic Retinal Camera NW500 Topcon Corporation


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