Elekta Limited

Elekta Limited — FDA 510(k) Submissions

Elekta Limited has submitted 8 FDA 510(k) premarket notifications since 2011, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Accelerator, Linear, Medical, Block, Beam-shaping, Radiation Therapy . Use the specialty filter in the sidebar to narrow results.