# K100056: Medcom RT-Viewer System

- Pathway: 510(k) (Traditional)
- Applicant: Medcom GmbH
- Decided: May 7, 2010 after 119 days
- Product code: MUJ (System, Planning, Radiation Therapy Treatment)
- Device class: 2
- Regulation: 21 CFR 892.5050
- 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
Bridge-RT is a Medical Device intended to be used for reviewing and assessment of DICOM based datasets which may occur in a radiotherapy environment. It is used by qualified specialist to load and display data generated by different DICOM devices including: RT-STRUCT, RT-PLAN, RT-OOSE, RT-IMAGE, CR, CT, MR and PET. The software provides the radiotherapy specialist with the necessary visualization and image manipulation tools to review, present or compare DlCOM, RT related datasets including the geometrical super imposition of 3D plan data. Bridge-RT is intended for reviewing purposes only and is not capable to generate new or modified RT plan data.

Source page: https://510kreport.com/device/K100056
Methodology: https://510kreport.com/methodology