Documento fuente o registro público

FDA 510(k) K243391 — AISight Dx

FDA 510(k) index record K243391. Device: AISight Dx. Applicant as listed: PathAI, Inc.. Decision date: 2025-06-26.

OtherU.S. Food and Drug Administration (FDA)2025-06-26

Fuente

"device_name": "AISight Dx"
api.fda.gov · Consultado el 2026-10-23

Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.

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Reviewer

Automated FDA record verification

Published

2026-10-20

Updated

2026-10-24

Disclaimer

professional use

References

FDA 510(k) public index record K243391.

Device name: AISight Dx. Applicant as listed: PathAI, Inc..

Decision date: 2025-06-26. 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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FDA 510(k) K243391 — AISight Dx

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