Angiolaz, Inc.

Angiolaz, Inc. — FDA 510(k) Submissions

Angiolaz, Inc. has submitted 10 FDA 510(k) premarket notifications since 1990, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Camera, Television, Endoscopic, Without Audio, Angioscope, Light Source, Endoscope, Xenon Arc, Light, Surgical, Floor Standing, Endoscopic Video Imaging System/component, Gastroenterology-urology . Use the specialty filter in the sidebar to narrow results.