Cleared Traditional

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

Oct 2021
Decision
217d
Days
Class 2
Risk

K210873 is an FDA 510(k) clearance for the Thermo Scientific Oxoid Lefamulin Disc (20µg) LMU20. This device is classified as a Susceptibility Test Discs, Antimicrobial (Class II - Special Controls, product code JTN).

Submitted by Oxoid Limited (Part of Thermo Fisher Scientific) (Basingstoke, GB). The FDA issued a Cleared decision on October 27, 2021, 217 days after receiving the submission on March 24, 2021.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.1620.

Submission Details

510(k) Number K210873 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 24, 2021
Decision Date October 27, 2021
Days to Decision 217 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Statement

Device Classification

Product Code JTN — Susceptibility Test Discs, Antimicrobial
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.1620

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