Source document or public record
FDA 510(k) K234012 — VITEK COMPACT PRO
FDA 510(k) index record K234012. Device: VITEK COMPACT PRO. Applicant as listed: bioMerieux, Inc.. Decision date: 2025-03-14.
Source
"device_name": "VITEK COMPACT PRO"
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 K234012.
Device name: VITEK COMPACT PRO. Applicant as listed: bioMerieux, Inc..
Decision date: 2025-03-14. Decision wording: Substantially Equivalent.
Product code: LON. Regulation: 21 CFR 866.1645. 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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