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

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.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.