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FDA 510(k) Applications Submitted by Lishan Aklog
FDA 510(k) Number
Submission Date
Device Name
Applicant
K210137
01/19/2021
EsoCheck Cell Collection Device
Lucid Diagnostics, Inc.
K200559
03/03/2020
CarpX
PAVmed, 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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