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FDA 510(k)

ARIA Radiation Therapy Management

K-Number: K173838 · 2018-01-17

ApplicantVarian Medical Systems, Inc.
Decision Date2018-01-17
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ARIA Radiation Therapy Management is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2018-01-17 under approval number K173838. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARIA Radiation Therapy Management?

ARIA Radiation Therapy Management is a medical device that received FDA 510(k) clearance on 2018-01-17. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K173838.

When was ARIA Radiation Therapy Management approved by the FDA?

ARIA Radiation Therapy Management received FDA 510(k) clearance on 2018-01-17, under approval number K173838.

What company makes ARIA Radiation Therapy Management?

ARIA Radiation Therapy Management is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for ARIA Radiation Therapy Management?

The FDA product code for ARIA Radiation Therapy Management is IYE.

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Related PubMed Literature

PMID: 41596046 A Review of 3D-Printed Medical Devices for Cancer Radiation Therapy. Bioengineering (Basel, Switzerland) (2026) PMID: 41052472 Successful management of recurrent multiple intracerebral TFE3-rearranged epithelioid hemangioendothelioma with repeated intervention and active surveillance: illustrative case. Journal of neurosurgery. Case lessons (2025) PMID: 40610624 Impact of a novel smartphone application for remote monitoring of gestational diabetes on glycaemic control and birth outcomes: a pilot observational study. Scientific reports (2025) PMID: 40036206 Glucosafe 2-A new tool for nutritional management and insulin-therapy in the intensive care unit: Randomized controlled study (the Glucosafe 2 protocol). PloS one (2025)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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