Lucid Diagnostics Inc

FDA Filings

This page includes the latest FDA filings for Lucid Diagnostics Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3016490370
FEI Number3016490370
NameLUCID DIAGNOSTICS, INC.
Owner & OperatorLucid Diagnostics, Inc.
Contact Address3 Allied Drive Suite 303
Dedham MA 02026 US
Official Correspondent
  • Richard D Yazbeck
  • 1-408-7310344-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3 Allied Drive Suite 303
Dedham, MA 02026 US
Establishment TypeComplaint File Establishment per 21 CFR 820.198

FDA Filings

Device
Company
DeviceDate
Lucid Diagnostics, Inc.
EsoCheck Cell Collection Device2022-10-26
Lucid Diagnostics, Inc.
EsoCheck Cell Collection Device2021-02-18
Lucid Diagnostics Inc
 EsoCheck CCD Cell Collection Device 2020-04-27
LUCID DIAGNOSTICS, INC.
EsoCheck2020-01-15
LUCID DIAGNOSTICS, INC.
EsoGuard Preservation Solution2020-01-15
Lucid Diagnostics, Inc.
EsoCheck CCD Cell Collection Device2019-06-21

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