Cleared Traditional

K123933 - MICROSCAN DRIED GRAM-POSITIVE MIC/COMBO PANELS - CEFTAROLINE (FDA 510(k) Clearance)

Mar 2013
Decision
84d
Days
Class 2
Risk

K123933 is an FDA 510(k) clearance for the MICROSCAN DRIED GRAM-POSITIVE MIC/COMBO PANELS - CEFTAROLINE. This device is classified as a Panels, Test, Susceptibility, Antimicrobial (Class II - Special Controls, product code LTT).

Submitted by Siemens Healthcare Diagnostics, Inc. (West Sacramento, US). The FDA issued a Cleared decision on March 14, 2013, 84 days after receiving the submission on December 20, 2012.

This device falls under the Microbiology FDA review panel. Regulated under 21 CFR 866.1640.

Submission Details

510(k) Number K123933 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 20, 2012
Decision Date March 14, 2013
Days to Decision 84 days
Submission Type Traditional
Review Panel Microbiology (MI)
Summary Summary PDF

Device Classification

Product Code LTT — Panels, Test, Susceptibility, Antimicrobial
Device Class Class II - Special Controls
CFR Regulation 21 CFR 866.1640