Nucletron Corporation

Nucletron Corporation — FDA 510(k) Submissions

Nucletron Corporation has submitted 19 FDA 510(k) premarket notifications since 2002, of which 19 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Applicator, Radionuclide, Remote-controlled, System, Planning, Radiation Therapy Treatment, System, Simulation, Radiation Therapy, Accelerator, Linear, Medical . Use the specialty filter in the sidebar to narrow results.