Siemens Receives FDA 510(K) Clearance for Next Generation Radiation Therapy Solution

CONCORD, Calif., Jan. 23 /PRNewswire/ -- Siemens Medical Solutions (www.usa.siemens.com/medical) announced it has received FDA 510(k) marketing clearance for the sale and distribution of its most recent innovation in radiation therapy technology, the ARTISTE(TM.

Developed by Siemens' Oncology Care Systems, the ARTISTE Solution is a linear accelerator engineered specifically for Adaptive Radiation Therapy (ART). Unique in design, ARTISTE is an integrated imaging and workflow solution that provides a comprehensive portfolio of image-guided and advanced treatment delivery protocols.

This new radiation therapy solution offers clinicians multiple imaging modalities. From Megavoltage (MV) to gold-standard, in-room CT imaging, clinicians can select the optimal imaging application for their treatment approach.

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