Source document or public record
FDA 510(k) K250968 — PathPresenter Clinical Viewer
FDA 510(k) index record K250968. Device: PathPresenter Clinical Viewer. Applicant as listed: Pathpresenter Corporation. Decision date: 2025-06-20.
Source
"device_name": "PathPresenter Clinical Viewer"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
Review and references
Automated FDA record verification
2026-10-20
2026-10-20
professional use
FDA 510(k) public index record K250968.
Device name: PathPresenter Clinical Viewer. Applicant as listed: Pathpresenter Corporation.
Decision date: 2025-06-20. Decision wording: Substantially Equivalent.
Product code: QKQ. Regulation: 21 CFR 864.3700. Medical specialty: Pathology.
This page reproduces regulator index metadata. The applicant field identifies the submitter and is not a manufacturer identity check. Consult the original FDA record for the decision and associated documents; this index does not verify current commercial availability or clinical performance.
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