Medical Device Manufacturer · US , New York , NY

Lucid Diagnostics, Inc. - FDA 510(k) Cleared Devices

4 submissions · 0 cleared · Since 2019

Total

Cleared

Denied

Lucid Diagnostics, Inc. has 0 FDA 510(k) cleared medical devices. Based in New York, US.

Last cleared in 2023. Active since 2019. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Lucid Diagnostics, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Lucid Diagnostics, Inc.

4 devices

1-4 of 4