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FDA 510(k)

Eclipse Treatment Planning System

K-Number: K181145 · 2018-05-18

ApplicantVarian Medical Systems, Inc.
Decision Date2018-05-18
Product CodeMUJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Eclipse Treatment Planning System is a medical device manufactured by Varian Medical Systems, Inc.. It received FDA 510(k) clearance on 2018-05-18 under approval number K181145. The device is classified under product code MUJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Eclipse Treatment Planning System?

Eclipse Treatment Planning System is a medical device that received FDA 510(k) clearance on 2018-05-18. It is manufactured by Varian Medical Systems, Inc.. The 510(k) number is K181145.

When was Eclipse Treatment Planning System approved by the FDA?

Eclipse Treatment Planning System received FDA 510(k) clearance on 2018-05-18, under approval number K181145.

What company makes Eclipse Treatment Planning System?

Eclipse Treatment Planning System is manufactured by Varian Medical Systems, Inc..

What is the FDA product code for Eclipse Treatment Planning System?

The FDA product code for Eclipse Treatment Planning System is MUJ.

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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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