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ARIA Radiation Therapy Management (v18.0)

K230699 Class II Special
Decision Date
2023-04-10
Sponsor / Applicant
Varian Medical Systems, Inc.

Technical Specification

510(k) Submission ID K230699
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2023-04-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARIA Radiation Therapy Management (v18.0) received FDA 510(k) clearance under submission number K230699, sponsored by Varian Medical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2023-04-10.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.