# K222719: CX50N

- Pathway: 510(k) (Traditional)
- Applicant: Wide Corporation
- Decided: May 9, 2023 after 243 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: 4 generations back to K103792 (2011). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170783: CX50N (CX50YQS), Wide Corporation (2017) Summary page 4.

## Indications for use
CX50N LCD Monitor System is intended to be used in displaying and viewing digital medical images for review and analysis by trained medical practitioners. It is specifically designed for digital mammography applications and digital breast tomosynthesis applications.

Source page: https://510kreport.com/device/K222719
Methodology: https://510kreport.com/methodology