FDA 510(k) Applications Submitted by LEICA BIOSYSTEMS IMAGING, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K232202 07/25/2023 Aperio GT 450 DX Leica Biosystems Imaging, Inc.
K190332 02/14/2019 Aperio AT2 DX System Leica Biosystems Imaging, Inc.
K141109 04/29/2014 APERIO EPATHOLOGY EIHC IVD SYSTEM LEICA BIOSYSTEMS IMAGING, INC.


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