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FDA 510(k)

Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System

K-Number: K182687 · 2018-11-23

Decision Date2018-11-23
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System is a medical device manufactured by Accuray Incorporated. It received FDA 510(k) clearance on 2018-11-23 under approval number K182687. 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 Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System?

Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System is a medical device that received FDA 510(k) clearance on 2018-11-23. It is manufactured by Accuray Incorporated. The 510(k) number is K182687.

When was Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System approved by the FDA?

Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System received FDA 510(k) clearance on 2018-11-23, under approval number K182687.

What company makes Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System?

Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System is manufactured by Accuray Incorporated.

What is the FDA product code for Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System?

The FDA product code for Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System is IYE.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.