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FDA 510(k)

Halcyon, Ethos Radiotherapy System

K-Number: K222941 · 2023-01-17

ApplicantVarian Medical Systems, Inc.
Decision Date2023-01-17
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Halcyon, Ethos Radiotherapy System is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2023-01-17 under approval number K222941. 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 Halcyon, Ethos Radiotherapy System?

Halcyon, Ethos Radiotherapy System is a medical device that received FDA 510(k) clearance on 2023-01-17. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K222941.

When was Halcyon, Ethos Radiotherapy System approved by the FDA?

Halcyon, Ethos Radiotherapy System received FDA 510(k) clearance on 2023-01-17, under approval number K222941.

What company makes Halcyon, Ethos Radiotherapy System?

Halcyon, Ethos Radiotherapy System is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for Halcyon, Ethos Radiotherapy System?

The FDA product code for Halcyon, Ethos Radiotherapy System 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.

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