Radius Intl., Inc.

Radius Intl., Inc. — FDA 510(k) Submissions

Radius Intl., Inc. has submitted 5 FDA 510(k) premarket notifications since 1995, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tubes, Gastrointestinal (and Accessories), Tube, Nasogastric, Wheelchair, Mechanical . Use the specialty filter in the sidebar to narrow results.