Source document or public record
FDA 510(k) K213626 — VITROS AFP
FDA 510(k) index record K213626. Device: VITROS AFP. Applicant as listed: Ortho Clinical Diagnostics. Decision date: 2022-06-15.
Source
"device_name": "VITROS AFP"
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 K213626.
Device name: VITROS AFP. Applicant as listed: Ortho Clinical Diagnostics.
Decision date: 2022-06-15. Decision wording: Substantially Equivalent.
Product code: LOJ. Regulation: 21 CFR 866.6010. Medical specialty: Immunology.
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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