# K142268: Varian Verification System (VVS)

- Pathway: 510(k) (Traditional)
- Applicant: Varian Medical Systems, Inc.
- Decided: Oct 2, 2014 after 48 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: 4 generations back to K001643 (2000). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091132: 4D Integrated Treatment Console, Varian Medical Systems (2009) Summary page 4.
- K103394: Barcode Conical Collimator Verification (BCCV), Varian Medical Systems, Oncology Systems (2011) Summary page 4.

## Indications for use
Varian Verification System is designed to assist the operator of a radiation therapy device in providing accurate treatment setups for each patient by monitoring the correct selection of patient, patient-specific accessories, conical collimator accessory and preventing the radiation treatment device from commencing irradiation when the selected patient, patient-specific accessories or conical collimator are out of conformance with the treatment plan.

Source page: https://510kreport.com/device/K142268
Methodology: https://510kreport.com/methodology