# K133994: SIVR56-T Kit

- Pathway: 510(k) (Traditional)
- Applicant: Barco N.V.
- Decided: Dec 1, 2014 after 340 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.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- 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
- K161880: NIVR58-T kit (2017), 0 descendants of its own

## Indications for use
The SIVR56-T KIT is intended to be used by healthcare professionals to integrate the video from various commercially available instruments commonly used in a medical procedure into a single video display.

Source page: https://510kreport.com/device/K133994
Methodology: https://510kreport.com/methodology