Bioimagene, Inc.

Bioimagene, Inc. — FDA 510(k) Submissions

Bioimagene, Inc. has submitted 3 FDA 510(k) premarket notifications since 2007, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include NOT, Microscope, Automated, Image Analysis, Immunohistochemistry,operator Intervention,nuclear Intensity & Percent Positivity . Use the specialty filter in the sidebar to narrow results.