Documento fuente o registro público

FDA 510(k) K250218 — Xpert® FII & FV

FDA 510(k) index record K250218. Device: Xpert® FII & FV. Applicant as listed: Cepheid. Decision date: 2025-02-21.

OtherU.S. Food and Drug Administration (FDA)2025-02-21

Fuente

"device_name": "Xpert® FII & FV"
api.fda.gov · Consultado el 2026-10-19

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

Review and references

Reviewer

Automated FDA record verification

Published

2026-10-20

Updated

2026-10-20

Disclaimer

professional use

References

FDA 510(k) public index record K250218.

Device name: Xpert® FII & FV. Applicant as listed: Cepheid.

Decision date: 2025-02-21. Decision wording: Substantially Equivalent.

Product code: NPR. Regulation: 21 CFR 864.7280. Medical specialty: Hematology.

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) K250218 — Xpert® FII & FV

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