Documento fuente o registro público
FDA 510(k) K220963 — Simplexa COVID-19 & Flu A/B Direct
FDA 510(k) index record K220963. Device: Simplexa COVID-19 & Flu A/B Direct. Applicant as listed: Diasorin Molecular, LLC. Decision date: 2023-03-17.
Fuente
"device_name": "Simplexa COVID-19 & Flu A/B Direct"
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
Automated FDA record verification
2026-10-20
2026-10-29
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FDA 510(k) public index record K220963.
Device name: Simplexa COVID-19 & Flu A/B Direct. Applicant as listed: Diasorin Molecular, LLC.
Decision date: 2023-03-17. 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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