Documento fuente o registro público

FDA 510(k) K261867 — Xpert Carba-R

FDA 510(k) index record K261867. Device: Xpert Carba-R. Applicant as listed: Cepheid®. Decision date: 2026-07-02.

OtherU.S. Food and Drug Administration (FDA)2026-07-02

Fuente

"device_name": "Xpert Carba-R"
api.fda.gov · Consultado el 2026-10-21

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

2026-10-22

Disclaimer

professional use

References

FDA 510(k) public index record K261867.

Device name: Xpert Carba-R. Applicant as listed: Cepheid®.

Decision date: 2026-07-02. Decision wording: Substantially Equivalent.

Product code: POC. Regulation: 21 CFR 866.1640. Medical specialty: Microbiology.

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) K261867 — Xpert Carba-R

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