Release date: 2008-02-20 Siemens linear accelerator is FDA certified
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On January 24th, Siemens Medical Development's conformal radiotherapy linear accelerator Artiste received US FDA 510(k) certification and entered the US market.
One of the highlights of Artiste's design is that the treatment bed can carry patients weighing up to 550 pounds. The Artiste system uses the syngo Suite, a radiation workflow developed by Siemens Medical for tumor radiotherapy. With the syngo Suite, you can get the data, patient information and related impact data needed for radiotherapy. ——China Medicine 123 Network
