# K122167: Nexxis or

- Pathway: 510(k) (Traditional)
- Applicant: Barco N.V.
- Decided: Apr 22, 2013 after 273 days
- Product code: DXJ (Display, Cathode-Ray Tube, Medical)
- Device class: 2
- Regulation: 21 CFR 870.2450
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K170537: Nexxis OR, Nexxis (2017), 2 descendants of its own
- K173381: Nexxis OR (2018), 1 descendant of its own
- K161122: Sony  IP Converter NU-IP40S (2016), 1 descendant of its own
- K261469: Nexxis 2;Nexxis OR 2;NMS 2;MNA-240;MNA-4x0 (Where “x” may be any numeric character). (2026), 0 descendants of its own
- K191678: IP Converter (2020), 0 descendants of its own

## Indications for use
The Barco Nexxis OR system is designed to allow transfer selection and distribution of A/V signals and medical images from various commercially available instruments that are commonly used in a medical procedure laboratory or operating room. The Barco, Nexxis OR system is also designed for transfer selection and distribution of human interface signals and control signals of non-medical room equipment. The Barco Nexxis OR system allows control and selection of these signals from a central point. The Barco Nexxis OR system is not intended to be used for remote or robotically-assisted surgery. The Barco, Nexxis OR system is not intended to be used in the vicinity of MRI or other devices that use strong magnetic fields.

Source page: https://510kreport.com/device/K122167
Methodology: https://510kreport.com/methodology