CMS gets 510(k) for I-Beam

Radiation therapy software provider CMS has received Food and Drug Administration 510(k) clearance for I-Beam, a mobile patient positioning system that employs ultrasound and other images to confirm the location of target organs or tumors. I-Beam uses 3-D positioning technology with an integrated camera and freehand ultrasound probe, which is registered through a passive localization target inserted in the shadow or wedge tray of any linear accelerator, according to the St. Louis-based firm.

By AuntMinnie.com staff writers
October 21, 2003

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