The Lighthouse For the Blind, Inc.

The Lighthouse For the Blind, Inc. — FDA 510(k) Submissions

The Lighthouse For the Blind, Inc. has submitted 2 FDA 510(k) premarket notifications since 1992, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Latex Patient Examination Glove, Device, Medical Examination, Ac Powered . Use the specialty filter in the sidebar to narrow results.