Siemens receives FDA 510(K) clearance for linear accelerator
Siemens Medical Solutions has received FDA 510(k) marketing clearance for the sale and distribution of Artiste, a linear accelerator engineered for adaptive radiation therapy.
Artiste's design features the 550 TxT Treatment Table, which Siemens said can accommodate a patient weight capacity of up to 550 pounds. The Artiste system is further enhanced by Siemens' syngo Suite for Oncology, a workflow platform providing scalable workspaces that enable clinical team members to access data, patient information and images as needed, according to Siemens.
Artiste's design features the 550 TxT Treatment Table, which Siemens said can accommodate a patient weight capacity of up to 550 pounds. The Artiste system is further enhanced by Siemens' syngo Suite for Oncology, a workflow platform providing scalable workspaces that enable clinical team members to access data, patient information and images as needed, according to Siemens.