Source document or public record
FDA 510(k) K210933 — YSI 2900C Biochemistry Analyzer
FDA 510(k) index record K210933. Device: YSI 2900C Biochemistry Analyzer. Applicant as listed: Ysi, Inc.. Decision date: 2024-09-30.
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"device_name": "YSI 2900C Biochemistry Analyzer"
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 K210933.
Device name: YSI 2900C Biochemistry Analyzer. Applicant as listed: Ysi, Inc..
Decision date: 2024-09-30. Decision wording: Substantially Equivalent.
Product code: CGA. Regulation: 21 CFR 862.1345. Medical specialty: Clinical Chemistry.
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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