Controlrad, Inc.

Controlrad, Inc. — FDA 510(k) Submissions

Controlrad, Inc. has submitted 6 FDA 510(k) premarket notifications since 2019, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Interventional Fluoroscopic X-ray System, Drape, Surgical . Use the specialty filter in the sidebar to narrow results.