Source document or public record
FDA 510(k) K241806 — Applied Biosystems TaqPath COVID-19, Flu A, Flu B, RSV Select Panel
FDA 510(k) index record K241806. Device: Applied Biosystems TaqPath COVID-19, Flu A, Flu B, RSV Select Panel. Applicant as listed: Life Technologies Corporation. Decision date: 2025-01-08.
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"device_name": "Applied Biosystems TaqPath COVID-19, Flu A, Flu B, RSV Select Panel"
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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2026-10-20
2026-10-20
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FDA 510(k) public index record K241806.
Device name: Applied Biosystems TaqPath COVID-19, Flu A, Flu B, RSV Select Panel. Applicant as listed: Life Technologies Corporation.
Decision date: 2025-01-08. 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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