# K243031: LCD Monitors C310S, G310S, C316S, G316S, C616W

- Pathway: 510(k) (Special)
- Applicant: Shenzhen Beacon Display Technology Co., Ltd.
- Decided: Oct 25, 2024 after 28 days
- Product code: PGY (Display, Diagnostic Radiology)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K000293 (2000). 17 ancestors in all.
No later device cites it as a predicate yet.
0 of 18 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K240310: LCD Monitors C310S, G310S, C316S, G316S, C616W, Shenzhen Beacon Display Technology Co., Ltd. (2024) Summary page 7.

## Indications for use
C310S, C316S and C616W are indicated for use in displaying radiological images for review, analysis, and diagnosis by trained medical practitioners. The displays are not intended for mammography. G310S and G316S are intended to be used in displaying and viewing digital images for diagnosis of X-ray or MRI, etc. by trained medical practitioners. The devices are not specified for digital mammography systems.

Source page: https://510kreport.com/device/K243031
Methodology: https://510kreport.com/methodology