Diacor, Inc.

Diacor, Inc. — FDA 510(k) Submissions

Diacor, Inc. has submitted 10 FDA 510(k) premarket notifications since 1986, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Accelerator, Linear, Medical, Monitor, Patient Position, Light-beam, Device, Patient Transfer, Powered, Block, Beam-shaping, Radiation Therapy . Use the specialty filter in the sidebar to narrow results.