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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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