FDA 510(k) Applications Submitted by Lucid Diagnostics, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K230339 02/07/2023 EsoCheck Cell Collection Device Lucid Diagnostics, Inc.
K210137 01/19/2021 EsoCheck Cell Collection Device Lucid Diagnostics, Inc.
K222366 08/04/2022 EsoCheck Cell Collection Device Lucid Diagnostics, Inc.
K183262 11/23/2018 EsoCheck CCD Cell Collection Device Lucid Diagnostics, Inc.


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