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# Fujifilm New CT System Cleared
- URL: https://www.fdaweb.com/fujifilm-new-ct-system-cleared/
- Published: 2024-06-26T12:00:00.000Z
- Updated: 2026-09-14T14:34:14.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5157255

FDA has cleared a Fujifilm Healthcare Americas 510(k) for its new compact, 128-slice computed tomography (CT) system, the FCT iStream. The device consolidates four core proprietary Fujifilm technologies, including HiMAR Plus (High image quality Metal Artifact Reduction), Intelli IPV, SynergyDrive and IntelliODM to “enhance the sharpness of images, streamline workflow through AI automation, and significantly reduce patient dose,” the company says.

“There is a clear need to decrease patient radiation dose as much as possible during imaging, including CT scans,” the company says. “The FCT iStream CT system comes equipped with several technologies that drive down patient dose, including Fujifilm’s IntelliODM, an-organ based dose modulation reduction technique which modulates radiation dose in angular and/or slice directions based on patient attenuation. Additionally, Fujifilm’s IntelliEC feature helps further reduce patient dose for all CT scanning, including cardiac imaging.”

The device can capture 60 images per second and uses Fujifilm’s SynergyDrive technology to automate, simplify and accelerate the scanning process, the company says. “SynergyDrive helps streamline the entire image capture process, assisting with automating positioning of the patient inside the CT system, mapping imaging parameters on where to scan, and scanning and archiving the images,” it says.