# K140956: LCD Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Nordicneurolab
- Decided: Aug 7, 2014 after 115 days
- Product code: LNH (System, Nuclear Magnetic Resonance Imaging)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K092253: Modification to Fmri Hardware System, Nordicneurolab (2009). Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Indications for use
The LCD monitor is intended to be used by trained professionals as a fMRI viewing monitor within the MR environment. This device must not be used for a life support system. This device must not be used for diagnostics.

Source page: https://510kreport.com/device/K140956
Methodology: https://510kreport.com/methodology