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FDA 510(k) K251978 — LIAISON NES FLU A/B, RSV & COVID-19
FDA 510(k) index record K251978. Device: LIAISON NES FLU A/B, RSV & COVID-19. Applicant as listed: Diasorin Molecular, LLC. Decision date: 2025-12-23.
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"device_name": "LIAISON NES FLU A/B, RSV & COVID-19"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
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Automated FDA record verification
2026-10-20
2026-10-20
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FDA 510(k) public index record K251978.
Device name: LIAISON NES FLU A/B, RSV & COVID-19. Applicant as listed: Diasorin Molecular, LLC.
Decision date: 2025-12-23. Decision wording: Substantially Equivalent.
Product code: QOF. Regulation: 21 CFR 866.3981. 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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