Lucid Diagnostics, Inc.

Lucid Diagnostics, Inc. — FDA 510(k) Submissions

Lucid Diagnostics, Inc. has submitted 4 FDA 510(k) premarket notifications since 2019, of which 0 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Esophagoscope (flexible Or Rigid) . Use the specialty filter in the sidebar to narrow results.