ARIA Radiation Therapy Management (v16.1 MR3)
K-Number: K221408 · 2022-06-17
ApplicantVarian Medical Systems, Inc.
Decision Date2022-06-17
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
ARIA Radiation Therapy Management (v16.1 MR3) is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2022-06-17 under approval number K221408. 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 (v16.1 MR3)?
ARIA Radiation Therapy Management (v16.1 MR3) is a medical device that received FDA 510(k) clearance on 2022-06-17. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K221408.
When was ARIA Radiation Therapy Management (v16.1 MR3) approved by the FDA?
ARIA Radiation Therapy Management (v16.1 MR3) received FDA 510(k) clearance on 2022-06-17, under approval number K221408.
What company makes ARIA Radiation Therapy Management (v16.1 MR3)?
ARIA Radiation Therapy Management (v16.1 MR3) is manufactured by Varian Medical Systems, Inc..
What is the FDA product code for ARIA Radiation Therapy Management (v16.1 MR3)?
The FDA product code for ARIA Radiation Therapy Management (v16.1 MR3) is IYE.
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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.