Siemens receives FDA nod for Artiste

AuntMinnie.com staff writers

Jan 23, 2008

Siemens Medical Solutions has received U.S. Food and Drug Administration (FDA) 510(k) clearance for its Artiste radiation therapy system.

Artiste is a linear accelerator designed to provide adaptive radiation therapy (ART), according to the Malvern, PA-based vendor. An integrated imaging and workflow package, Artiste offers a portfolio of image-guided and treatment delivery protocols, Siemens said.

Related Reading

Siemens loses first round in Saint-Gobain suit, January 14, 2008

Siemens Medical changes corporate name, January 10, 2008

London hospital to install Siemens' 3-tesla MRI unit, January 10, 2008

InSiteOne wraps up Siemens validation, January 10, 2008

Siemens unveils Artiste, October 4, 2004

Copyright © 2008 AuntMinnie.com

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