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FDA 510(k)

Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0)

K-Number: K232923 · 2024-04-30

ApplicantVarian Medical Systems, Inc.
Decision Date2024-04-30
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0) is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2024-04-30 under approval number K232923. 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 Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0)?

Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0) is a medical device that received FDA 510(k) clearance on 2024-04-30. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K232923.

When was Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0) approved by the FDA?

Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0) received FDA 510(k) clearance on 2024-04-30, under approval number K232923.

What company makes Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0)?

Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0) is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0)?

The FDA product code for Ethos Treatment Management (3.0); Ethos Treatment Planning (2.0) 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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