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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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