Cleared Traditional

K921193 - LOMEFLOXACIN, 10 MCG, SENSI DISC (FDA 510(k) Clearance)

Apr 1992
Decision
46d
Days
Class 2
Risk

K921193 is an FDA 510(k) clearance for the LOMEFLOXACIN, 10 MCG, SENSI DISC. This device is classified as a Susceptibility Test Discs, Antimicrobial (Class II - Special Controls, product code JTN).

Submitted by Bd Becton Dickinson Vacutainer Systems Preanalytic (Cockeysville, US). The FDA issued a Cleared decision on April 27, 1992, 46 days after receiving the submission on March 12, 1992.

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

Submission Details

510(k) Number K921193 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 12, 1992
Decision Date April 27, 1992
Days to Decision 46 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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