FDA clears KinetiCor's MRI motion correction system

By AuntMinnie.com staff writers

February 24, 2020 -- The U.S. Food and Drug Administration (FDA) has cleared KinetiCor's MRI optical motion correction system for use with Siemens Healthineers' Magnetom Skyra 3-tesla scanner.

The KinetiCor Motion Correction system will be used as an accessory to Siemens' scanner, allowing users to track patient movement during an MRI exam and adjust the images as needed, according to KinetiCor.

In other KinetiCor news, the company has named Michael Jones as chair of its board of advisors. Jones comes to KinetiCor with more than 21 years of experience at GE Healthcare.

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