Omega Medical Imaging, Inc.

Omega Medical Imaging, Inc. — FDA 510(k) Submissions

Omega Medical Imaging, Inc. has submitted 8 FDA 510(k) premarket notifications since 1990, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Interventional Fluoroscopic X-ray System, System, X-ray, Fluoroscopic, Image-intensified, Collimator, Automatic, Radiographic . Use the specialty filter in the sidebar to narrow results.