Kent Imaging, Inc.

Kent Imaging, Inc. — FDA 510(k) Submissions

Kent Imaging, Inc. has submitted 4 FDA 510(k) premarket notifications since 2012, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Oximeter, Tissue Saturation, Autofluorescence Imaging Adjunct Tool For Wounds . Use the specialty filter in the sidebar to narrow results.