Home » Varian Receives FDA 510(k) Clearance for RapidArc
Varian Receives FDA 510(k) Clearance for RapidArc
The FDA has granted 510(k) clearances for Varian Medical Systems’ RapidArc radiotherapy technology.
The technology will deliver image-guided, intensity-modulated radiation therapy (IMRT) two to eight times faster than conventional IMRT or helical tomotherapy.
Studies comparing fixed-beam RapidArc with helical IMRT show that RapidArc can reduce the amount of nontherapeutic radiation reaching healthy tissues during treatment, according to Varian.
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