Eizo Corporation

Eizo Corporation — FDA 510(k) Submissions

Eizo Corporation has submitted 29 FDA 510(k) premarket notifications since 2013, of which 29 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Display, Diagnostic Radiology, System, Image Processing, Radiological, Laparoscope, General & Plastic Surgery, Digital Pathology Display . Use the specialty filter in the sidebar to narrow results.