Source document or public record

FDA 510(k) K210873 — Thermo Scientific Oxoid Lefamulin Disc (20µg) LMU20

FDA 510(k) index record K210873. Device: Thermo Scientific Oxoid Lefamulin Disc (20µg) LMU20. Applicant as listed: Oxoid Limited (Part of Thermo Fisher Scientific). Decision date: 2021-10-27.

OtherU.S. Food and Drug Administration (FDA)2021-10-27

Source

"device_name": "Thermo Scientific Oxoid Lefamulin Disc (20µg) LMU20"

This entry describes what the document covers; the document itself is the authority. Listing it is not agreement with its conclusions.

Review and references

Reviewer

Automated FDA record verification

Published

2026-10-20

Updated

2026-10-20

Disclaimer

professional use

FDA 510(k) public index record K210873.

Device name: Thermo Scientific Oxoid Lefamulin Disc (20µg) LMU20. Applicant as listed: Oxoid Limited (Part of Thermo Fisher Scientific).

Decision date: 2021-10-27. Decision wording: Substantially Equivalent.

Product code: JTN. Regulation: 21 CFR 866.1620. 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.

Interested in these solutions?

Submit a sourcing request with the assays, volumes, and timeline of your own project.