# K160346: MX30N (MX30TQS)

- Pathway: 510(k) (Traditional)
- Applicant: Wide Corporation
- Decided: Apr 14, 2016 after 66 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: 3 generations back to K001753 (2000). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032174: Wide 3MP Grayscale TFT LCD Monitor IF2103A, Wide Corporation (2003) Summary page 4.

## Indications for use
The MX30N(MX30TQS) LCD Monitor System is intended to be used in displaying and viewing digital medical images for review and analysis by trained medical practitioners. The display is not intended for mammography.

Source page: https://510kreport.com/device/K160346
Methodology: https://510kreport.com/methodology