# K260733: MRIA Radiation Therapy Information System (MRIA)

- Pathway: 510(k) (Traditional)
- Applicant: Manteia Technologies Co., Ltd.
- Decided: Aug 26, 2026 after 173 days
- Product code: IYE (Accelerator, Linear, Medical)
- 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
Longest line of descent: 8 generations back to K952313 (1995). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K242463: ARIA Radiation Therapy Management System (18.1), Varian Medical Systems, Inc. (2024) Summary page 5.

## Indications for use
MRIA is a radiation therapy information system, mainly for doctors, physicists, technologists and administrators in the radiotherapy department of hospitals to solve the problem of inconvenient information interaction in their positioning, contouring, planning and treatment sessions. MRIA is not a treatment planning system or a radiation delivery device. It is used only for process progress management and treatment information management for radiotherapy patients.

Source page: https://510kreport.com/device/K260733
Methodology: https://510kreport.com/methodology