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Clinical Trials
3
1 active
Approvals
0
Total approvals
Agencies
Regulatory bodies
Founded
N/A
No trial phase data available
Active, not recruiting
1
33.3%
Completed
Terminated
No approval data available
- PathPresenter has received FDA 510(k) clearance for its Clinical Viewer platform, enabling primary diagnosis using digital pathology workflows. - The clearance is specifically for use with Hamamatsu NanoZoomer S360MD slide scanners and Barco NV MDPC-8127 display devices. - The platform addresses a critical need in healthcare, as pathology guides nearly 70% of clinical decision-making processes. - This regulatory milestone advances the adoption of digital workflows in pathology and supports precision medicine initiatives.
