Lkc Technologies, Inc.

Lkc Technologies, Inc. — FDA 510(k) Submissions

Lkc Technologies, Inc. has submitted 8 FDA 510(k) premarket notifications since 1976, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tester, Color Vision, Anomaloscope, Photostimulator, Ac-powered, Stimulator, Photic, Evoked Response, Electrode, Corneal . Use the specialty filter in the sidebar to narrow results.