Documento fuente o registro público

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.

OtherU.S. Food and Drug Administration (FDA)2022-07-27

Fuente

"device_name": "EliA Ro52, EliA Ro60"
api.fda.gov · Consultado el 2026-10-29

Esta entrada describe lo que cubre el documento; el propio documento es la autoridad. Incluirlo no implica estar de acuerdo con sus conclusiones.

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Reviewer

Automated FDA record verification

Published

2026-10-20

Updated

2026-10-30

Disclaimer

professional use

References

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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FDA 510(k) K210902 — EliA Ro52, EliA Ro60

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