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FDA 510(k)

Xpert Xpress CoV-2/Flu plus

K-Number: K263120 · 2026-10-02

ApplicantCepheid®
Decision Date2026-10-02
Product CodeQOF
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

Xpert Xpress CoV-2/Flu plus is the device name listed in this FDA 510(k) record. The listed applicant is Cepheid®. It received FDA 510(k) clearance on 2026-10-02 under 510(k) number K263120. The device is classified under product code QOF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Xpert Xpress CoV-2/Flu plus?

Xpert Xpress CoV-2/Flu plus is a medical device that received FDA 510(k) clearance on 2026-10-02. The listed applicant is Cepheid®. The 510(k) number is K263120.

When did Xpert Xpress CoV-2/Flu plus receive FDA 510(k) clearance?

Xpert Xpress CoV-2/Flu plus received FDA 510(k) clearance on 2026-10-02, under 510(k) number K263120.

Who is the listed applicant for Xpert Xpress CoV-2/Flu plus?

The FDA 510(k) record lists Cepheid® as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Xpert Xpress CoV-2/Flu plus?

The FDA product code for Xpert Xpress CoV-2/Flu plus is QOF.

Related Clinical Trials

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Other records listing Cepheid® as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261336Xpert Respiratory PanelK261362Xpert Hemorrhagic FeverK261867Xpert Carba-RK253653Xpert Hemorrhagic FeverK251721Xpert GI PanelK250995Xpert Xpress CoV-2/Flu/RSV plus

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Related Devices (Code: QOF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261336Xpert Respiratory PanelCepheidK263054BIOFIRE Respiratory Panel 2.1 (RP2.1)Biofire DiagnosticsK261837FINDER Flu A&B/SARS-CoV-2 TestBaebies, Inc.K252932Fast PCR Mini Respiratory PanelAutonomous Medical Devices IncorporatedK252269FINDER Flu A&B/SARS-CoV-2 TestBaebies, Inc.K251742VELO Respiratory TestLex Diagnostics Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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