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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 the device name listed in this FDA 510(k) record. The listed applicant is Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2024-12-13 under 510(k) 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. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K242463.

When did ARIA Radiation Therapy Management System (18.1) receive FDA 510(k) clearance?

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

Who is the listed applicant for ARIA Radiation Therapy Management System (18.1)?

The FDA 510(k) record lists Varian Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Varian Medical Systems, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 96 devices →

Related Devices (Code: MUJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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