Source document or public record
FDA 510(k) K231020 — Alinity c Tricyclic Antidepressants Reagent Kit
FDA 510(k) index record K231020. Device: Alinity c Tricyclic Antidepressants Reagent Kit. Applicant as listed: Microgenics Corporation. Decision date: 2023-11-17.
Source
"device_name": "Alinity c Tricyclic Antidepressants Reagent Kit"
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 K231020.
Device name: Alinity c Tricyclic Antidepressants Reagent Kit. Applicant as listed: Microgenics Corporation.
Decision date: 2023-11-17. Decision wording: Substantially Equivalent.
Product code: LFH. Regulation: 21 CFR 862.3910. Medical specialty: Clinical Toxicology.
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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