Cleared Traditional

LCD Monitors C310S, G310S, C316S, G316S, C616W

K240310 · Shenzhen Beacon Display Technology Co., Ltd. · Radiology

Mar 2024

Decision

56d

Days

Class 2

Risk

About This 510(k) Submission

K240310 is an FDA 510(k) clearance for the LCD Monitors C310S, G310S, C316S, G316S, C616W, a Display, Diagnostic Radiology (Class II — Special Controls, product code PGY), submitted by Shenzhen Beacon Display Technology Co., Ltd. (Shenzhen, CN). The FDA issued a Cleared decision on March 29, 2024, 56 days after receiving the submission on February 2, 2024. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2050.

Submission Details

510(k) Number	K240310 FDA.gov
FDA Decision	Cleared SESE
Date Received	February 02, 2024
Decision Date	March 29, 2024
Days to Decision	56 days
Submission Type	Traditional
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.