# K133984: Coronis 5MP

- Pathway: 510(k) (Traditional)
- Applicant: Barco N.V.
- Decided: Mar 28, 2014 after 92 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
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. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Coronis 5MP (MDCG-5221) display is intended to be used in displaying and viewing digital images, for review and analysis by trained medical practitioners. It is designed for radiology and digital mammography applications.

Source page: https://510kreport.com/device/K133984
Methodology: https://510kreport.com/methodology