Source document or public record
FDA 510(k) K222829 — Curian® Shiga Toxin
FDA 510(k) index record K222829. Device: Curian® Shiga Toxin. Applicant as listed: Meridian Bioscience, Inc.. Decision date: 2023-04-17.
Source
"device_name": "Curian® Shiga Toxin"
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 K222829.
Device name: Curian® Shiga Toxin. Applicant as listed: Meridian Bioscience, Inc..
Decision date: 2023-04-17. Decision wording: Substantially Equivalent.
Product code: GMZ. Regulation: 21 CFR 866.3255. 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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