Class Class II

PathPresenter Clinical Viewer (K250968)

K250968 2025-06-20 Traditional
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Description

PathPresenter Clinical Viewer by Pathpresenter Corporation — FDA 510(k) cleared pathology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250968
Clearance Date2025-06-20
Clearance TypeTraditional
Product CodeQKQ
Regulation Number864.3700

Categories

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