Cleared Traditional

K131090 - 2MP COLOR LCD MONITOR, RADIFORCE MX215 (FDA 510(k) Clearance)

Jul 2013
Decision
76d
Days
Class 2
Risk

K131090 is an FDA 510(k) clearance for the 2MP COLOR LCD MONITOR, RADIFORCE MX215. This device is classified as a System, Image Processing, Radiological (Class II - Special Controls, product code LLZ).

Submitted by Eizo Corporation (Hakusan, Ishikawa, JP). The FDA issued a Cleared decision on July 3, 2013, 76 days after receiving the submission on April 18, 2013.

This device falls under the Radiology FDA review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number K131090 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 18, 2013
Decision Date July 03, 2013
Days to Decision 76 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code LLZ — System, Image Processing, Radiological
Device Class Class II - Special Controls
CFR Regulation 21 CFR 892.2050