# K190831: E240AG LCD Monitor, E240A LCD Monitor, JUSHA-E240AG LCD Monitor, JUJSHA-E240A LCD Monitor, C230A LCD Monitor, JUSHA-C230A LCD Monitor, C230M LCD Monitor, JUSHA-C230M LCD Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Nanjing Jusha Display Technology Co., Ltd.
- Decided: May 31, 2019 after 60 days
- Product code: GCJ (Laparoscope, General & Plastic Surgery)
- Device class: 2
- Regulation: 21 CFR 876.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K943305 (1995). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113203: Sony LMD-2451MT LCD Monitor, Sony Electronics, Inc. (2012) Summary page 4.

## Indications for use
The E240AG LCD Monitor is intended to provide 2D color video displays of images from surgical endoscopic/laparoscopic camera systems and other compatible medical imaging systems. The E240AG is a widescreen, high definition, medical grade monitor for real-time use during minimally invasive surgical procedures and is suitable for use in hospital operating rooms, surgical centers, clinics, doctors' offices and similar medical environments.

Source page: https://510kreport.com/device/K190831
Methodology: https://510kreport.com/methodology