Konica Minolta, Inc.

Konica Minolta, Inc. — FDA 510(k) Submissions

Konica Minolta, Inc. has submitted 25 FDA 510(k) premarket notifications since 2014, of which 25 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Solid State X-ray Imager (flat Panel/digital Imager), System, Image Processing, Radiological, System, Imaging, Pulsed Doppler, Ultrasonic, System, Imaging, Pulsed Echo, Ultrasonic . Use the specialty filter in the sidebar to narrow results.