Leica Biosystems Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Aperio GT 450 DX, Aperio iQC DX Software, Aperio GT 450 DX
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Leica Biosystems Imaging, Inc. Pathology ✕
5 devices