QVA — Fludeoxyglucose F18-Guided Radiation Therapy System Class II

FDA Device Classification

Classification Details

Product Code
QVA
Device Class
Class II
Regulation Number
892.5060
Submission Type
Review Panel
RA
Medical Specialty
Radiology
Implant
No

Definition

A fludeoxyglucose F18-guided radiation therapy system is a device that combines the functionality of an emission computed tomography detection system and a linear accelerator. The device is intended for use with approved fludeoxyglucose F18. The emission computed tomography detection system acquires images of positron-emitting fludeoxyglucose F18 for the purpose of guiding the delivery of megavoltage X-rays for oncologic treatment with radiation therapy using an FDA cleared, authorized, or approved linear accelerator.

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K252071reflexion medicalRefleXion Medical Radiotherapy System, Reflexion X2December 18, 2025
DEN220014reflexion medicalRefleXion Medical Radiotherapy System (RMRS)February 1, 2023