510(k) K240310

LCD Monitors C310S, G310S, C316S, G316S, C616W by Shenzhen Beacon Display Technology Co., Ltd. — Product Code PGY

K240310 is an FDA 510(k) premarket notification submitted by Shenzhen Beacon Display Technology Co., Ltd. for the device "LCD Monitors C310S, G310S, C316S, G316S, C616W". The FDA issued a decision of Substantially Equivalent on March 29, 2024. The device falls under product code PGY (Display, Diagnostic Radiology), a Class II device regulated under 21 CFR 892.2050. Shenzhen Beacon Display Technology Co., Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 29, 2024
Date Received
February 2, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Display, Diagnostic Radiology
Device Class
Class II
Regulation Number
892.2050
Review Panel
RA
Submission Type

The device is intended for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners.