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FDA 510(k)

Ethos Treatment Management, Ethos Treatment Planning

K-Number: K212294 · 2021-08-20

ApplicantVarian Medical Systems, Inc.
Decision Date2021-08-20
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Ethos Treatment Management, Ethos Treatment Planning 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 2021-08-20 under 510(k) number K212294. 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, Ethos Treatment Planning?

Ethos Treatment Management, Ethos Treatment Planning is a medical device that received FDA 510(k) clearance on 2021-08-20. The listed applicant is Varian Medical Systems, Inc.. The 510(k) number is K212294.

When did Ethos Treatment Management, Ethos Treatment Planning receive FDA 510(k) clearance?

Ethos Treatment Management, Ethos Treatment Planning received FDA 510(k) clearance on 2021-08-20, under 510(k) number K212294.

Who is the listed applicant for Ethos Treatment Management, Ethos Treatment Planning?

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 Ethos Treatment Management, Ethos Treatment Planning?

The FDA product code for Ethos Treatment Management, Ethos Treatment Planning is IYE.

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Other records listing Varian Medical Systems, Inc. as applicant

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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.

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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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