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See today's BioWorld MedTech
Home » FDA clears major upgrade to Elekta’s MR-Linac system
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FDA clears major upgrade to Elekta’s MR-Linac system

March 17, 2023
By David Godkin
Elekta AB received U.S. FDA clearance for what it called a “groundbreaking upgrade” of its MR-Linac platform which can continuously calculate the movement of a tumor anywhere in the body. The company said the Elekta Unity’s comprehensive motion management platform provides clinicians with enhanced, adaptive radiation therapy workflow to track moving organs such as the prostate, liver and pancreas.
BioWorld MedTech Regulatory Imaging U.S. 510(k) FDA

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