Cleared Special

Nio Color 8MP (MDNC-8132)

K233693 · Barco N.V. · Radiology

Dec 2023

Decision

24d

Days

Class 2

Risk

About This 510(k) Submission

K233693 is an FDA 510(k) clearance for the Nio Color 8MP (MDNC-8132), a Display, Diagnostic Radiology (Class II — Special Controls, product code PGY), submitted by Barco N.V. (Kortrijk, BE). The FDA issued a Cleared decision on December 11, 2023, 24 days after receiving the submission on November 17, 2023. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number	K233693 FDA.gov
FDA Decision	Cleared SESE
Date Received	November 17, 2023
Decision Date	December 11, 2023
Days to Decision	24 days
Submission Type	Special
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.