Gammex, Inc.

Gammex, Inc. — FDA 510(k) Submissions

Gammex, Inc. has submitted 3 FDA 510(k) premarket notifications since 1995, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Monitor, Patient Position, Light-beam, System, Digital Image Communications, Radiological, Accelerator, Linear, Medical . Use the specialty filter in the sidebar to narrow results.