FDA OKs software upgrades to Toshiba's Aquilion One

Toshiba America Medical Systems has received U.S. Food and Drug Administration (FDA) clearance for a new package of detector and software enhancements to its Aquilion One family of CT systems.

The version 7.0 package includes the following:

  • AIDR 3D Enhanced, Toshiba's fourth-generation adaptive iterative dose reduction algorithm
  • Its PureVision CT detector, with 40% better light output for improved use of x-ray photons
  • SurekV automated kV selection based on patient size
  • Organ effective modulation, which limits dose to radiosensitive organs and also during helical scanning and CT fluoroscopy procedures
  • Contrast management features that improve workflow and safety by standardizing contrast protocols and automatically tracking volume of contrast used during an exam
  • A power save mode that includes a sleep mode option for when the CT system is not in use
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