FDA 510(k)

ARIA Radiation Therapy Management System (18.1)

K-Number: K242463 · 2024-12-13

Decision Date2024-12-13

Product CodeMUJ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ARIA Radiation Therapy Management System (18.1) is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2024-12-13 under approval number K242463. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARIA Radiation Therapy Management System (18.1)?

ARIA Radiation Therapy Management System (18.1) is a medical device that received FDA 510(k) clearance on 2024-12-13. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K242463.

When was ARIA Radiation Therapy Management System (18.1) approved by the FDA?

ARIA Radiation Therapy Management System (18.1) received FDA 510(k) clearance on 2024-12-13, under approval number K242463.

What company makes ARIA Radiation Therapy Management System (18.1)?

ARIA Radiation Therapy Management System (18.1) is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for ARIA Radiation Therapy Management System (18.1)?

The FDA product code for ARIA Radiation Therapy Management System (18.1) is MUJ.

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Related PubMed Literature

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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.