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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 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 2018-01-17 under 510(k) 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. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K173838.

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

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

Who is the listed applicant for ARIA Radiation Therapy Management?

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?

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

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.

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Related Devices (Code: IYE)

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.

K261856Halcyon, Ethos Radiotherapy System (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SAK253004LUNA 3DLap GmbH Laser ApplikationenK260792AerFrame Patient Immobilization System (AFPIS)Stabilix, LLCK252258VERIQA RT EPID 3DPtw-Freiburg Physikalisch-Technische-Werkstaetten Dr. PychlaK253962ClearCheck (RADCC V2.7)Radformation, Inc.

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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