FDA 510(k) Applications Submitted by Yuko Matsushita

FDA 510(k) Number Submission Date Device Name Applicant
K250553 02/25/2025 Tomey Cornea/Anterior Segment OCT (CASIA2) TOMEY Corporation
K213265 09/30/2021 Tomey Cornea/Anterior Segment OCT CASIA2 Tomey Corporation


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