Cleared Abbreviated

RadiForce RX360, RX360-AR

K182591 · Eizo Corporation · Radiology

Oct 2018

Decision

28d

Days

Class 2

Risk

About This 510(k) Submission

K182591 is an FDA 510(k) clearance for the RadiForce RX360, RX360-AR, a Display, Diagnostic Radiology (Class II — Special Controls, product code PGY), submitted by Eizo Corporation (Hakusan, JP). The FDA issued a Cleared decision on October 18, 2018, 28 days after receiving the submission on September 20, 2018. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number	K182591 FDA.gov
FDA Decision	Cleared SESE
Date Received	September 20, 2018
Decision Date	October 18, 2018
Days to Decision	28 days
Submission Type	Abbreviated
Review Panel	Radiology (RA)
Summary	Summary PDF

Device Classification

Product Code	PGY — Display, Diagnostic Radiology
Device Class	Class II — Special Controls
CFR Regulation	21 CFR 892.2050
Definition	The Device Is Intended For Use In Displaying Radiological Images For Review, Analysis, And Diagnosis By Trained Medical Practitioners.