Cleared Traditional

K183127 - MicroScan Dried Gram Negative MIC/Combo Panels with Meropenem/Vaborbactam (0.03/8-64/8ug/mL) (FDA 510(k) Clearance)

Feb 2019
Decision
91d
Days
Class 2
Risk

K183127 is an FDA 510(k) clearance for the MicroScan Dried Gram Negative MIC/Combo Panels with Meropenem/Vaborbactam (0.03/8-64/8ug/mL). This device is classified as a Panels, Test, Susceptibility, Antimicrobial (Class II - Special Controls, product code LTT).

Submitted by Beckman Coulter, Inc. (West Sacramento, US). The FDA issued a Cleared decision on February 12, 2019, 91 days after receiving the submission on November 13, 2018.

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

Submission Details

510(k) Number K183127 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 13, 2018
Decision Date February 12, 2019
Days to Decision 91 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