# K160355: CX20N (CX20PUX)

- Pathway: 510(k) (Traditional)
- Applicant: Wide Corporation
- Decided: Apr 7, 2016 after 59 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 K001753 (2000). 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)
- K032960: Wide 2MP TFT LCD Monitor System IF 1902A, Wide Corporation (2003) Summary page 4.

## Indications for use
The CX20N(CX20PUX) LCD Monitor System is intended to be used in displaying and viewing digital medical images for review and analysis by trained medical practitioners.

Source page: https://510kreport.com/device/K160355
Methodology: https://510kreport.com/methodology