# K023533: Barco Medis 5MP2 Aura

- Pathway: 510(k) (Traditional)
- Applicant: Barco N.V.
- Decided: Jan 17, 2003 after 88 days
- Product code: LLZ (System, Image Processing, Radiological)
- 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: 1 generation back to K001748 (2000). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001748: Medis 5MP2 Quad-Head Medical Diagnostic Display System, Barco NV Display Systems (2000)

## Indications for use
The MeDis 5MP2 Aura is intended to be used in displaying and viewing digital images for review and analysis by trained medical practitioners.

Source page: https://510kreport.com/device/K023533
Methodology: https://510kreport.com/methodology