FDA 510(k) Applications Submitted by Tomey Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K073087 11/01/2007 NON-CONTACT TONOMETER, MODEL FT-1000 TOMEY CORPORATION
K171313 05/04/2017 EM-4000 Specular Microscope Tomey Corporation
K213265 09/30/2021 Tomey Cornea/Anterior Segment OCT CASIA2 Tomey Corporation


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