Cleared Traditional

K162740 - MicroScan Dried Gram-Negative MIC/Combo Panels with Imipenem (0.25 - 8 ug/mL) (FDA 510(k) Clearance)

Mar 2017
Decision
172d
Days
Class 2
Risk

K162740 is an FDA 510(k) clearance for the MicroScan Dried Gram-Negative MIC/Combo Panels with Imipenem (0.25 - 8 ug/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 March 21, 2017, 172 days after receiving the submission on September 30, 2016.

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

Submission Details

510(k) Number K162740 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 30, 2016
Decision Date March 21, 2017
Days to Decision 172 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