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ARIA RADIATION THERAPY MANAGEMENT

K133572 Class II Traditional
Decision Date
2014-04-04
Sponsor / Applicant
Varian Medical Systems, Inc.

Technical Specification

510(k) Submission ID K133572
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2014-04-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ARIA RADIATION THERAPY MANAGEMENT received FDA 510(k) clearance under submission number K133572, sponsored by Varian Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2014-04-04.

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.