# K124002: Verification Console

- Pathway: 510(k) (Traditional)
- Applicant: Varian Medical Systems
- Decided: Feb 21, 2013 after 57 days
- Product code: LHN (System, Radiation Therapy, Charged-Particle, 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: 2 generations back to K872369 (1988). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K082416: Iba Proton Therapy System- Proteus 235, Ion Beam Applications S.A. (2008) Summary page 1.

## Indications for use
Verification Console is designed to assist the operator of a proton radiation therapy device. Verification Console retrieves treatment plans from an oncology information system (01S) and sends plans to the treatment device's treatment control system (TCS). Verification Console then performs verification of treatment plan parameters against TCS delivery parameters for accuracy prior to beam authorization, and sends the treatment history for recording to the 015.

Source page: https://510kreport.com/device/K124002
Methodology: https://510kreport.com/methodology