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 Number: 3016490370
• FEI Number: 3016490370
• Name: LUCID DIAGNOSTICS, INC.
• Owner & Operator: Lucid Diagnostics, Inc.
• Contact Address: 3 Allied Drive Suite 303; Dedham MA 02026 US
• Official Correspondent:
  • Richard D Yazbeck
  • 1-408-7310344-x
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 3 Allied Drive Suite 303; Dedham, MA 02026 US
• Establishment Type: Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device Company	Device	Date
PMN K222366 Lucid Diagnostics, Inc.	EsoCheck Cell Collection Device	2022-10-26
PMN K210137 Lucid Diagnostics, Inc.	EsoCheck Cell Collection Device	2021-02-18
GUDID 00860002356013 Lucid Diagnostics Inc	EsoCheck CCD Cell Collection Device	2020-04-27
PMN K183262 | EOX LUCID DIAGNOSTICS, INC.	EsoCheck	2020-01-15
NNK LUCID DIAGNOSTICS, INC.	EsoGuard Preservation Solution	2020-01-15
PMN K183262 Lucid Diagnostics, Inc.	EsoCheck CCD Cell Collection Device	2019-06-21