Source document or public record
FDA 510(k) K210902 — EliA Ro52, EliA Ro60
FDA 510(k) index record K210902. Device: EliA Ro52, EliA Ro60. Applicant as listed: Phadia AB. Decision date: 2022-07-27.
Source
"device_name": "EliA Ro52, EliA Ro60"
This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.
Review and references
Automated FDA record verification
2026-10-20
2026-10-20
professional use
FDA 510(k) public index record K210902.
Device name: EliA Ro52, EliA Ro60. Applicant as listed: Phadia AB.
Decision date: 2022-07-27. Decision wording: Substantially Equivalent.
Product code: LKJ. Regulation: 21 CFR 866.5100. 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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