# K252258: Veriqa RT Epid 3D

- Pathway: 510(k) (Traditional)
- Applicant: Ptw-Freiburg Physikalisch-Technische-Werkstaetten Dr. Pychla
- Decided: Apr 15, 2026 after 268 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: 5 generations back to K914698 (1992). 13 ancestors in all.
No later device cites it as a predicate yet.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141800: Perfraction, Sun Nuclear Corporation (2014) Summary page 5.

## Indications for use
Software for quality assurance of ionizing radiation emitted by diagnostic imaging devices or radiotherapy devices. VERIQA RT EPID 3D is a software to assist the user in detecting errors related to – treatment planning, – plan delivery by the treatment machine, – changes in the patient anatomy, and/or patient setup deviations. VERIQA RT EPID 3D must not be used to modify a patient´s treatment plan based exclusively on the results from VERIQA RT EPID 3D. VERIQA RT EPID 3D must not be used for treatment planning. The clinical user of VERIQA RT EPID 3D is the medical physicist. Transport tasks are performed by the carrier. PTW service staff is responsible for service tasks.

Source page: https://510kreport.com/device/K252258
Methodology: https://510kreport.com/methodology