Medical Device Manufacturer · US , New York , NY

Lucid Diagnostics, Inc.

4 submissions · 0 cleared · Since 2019
4
Total
0
Cleared
0
Denied

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.

4 devices
1–4 of 4
Filters