EsoCheck Cell Collection Device— 510(k) K230339

Unknown

Lucid Diagnostics, Inc.

FDA 510(k) clearance K230339 for EsoCheck Cell Collection Device, Unknown on 2023-02-24. Applicant: Lucid Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Lucid Diagnostics, Inc.
Product code: Code EOX
Device class: Class 2
Regulation: 21 CFR 874.4710
Advisory panel: Ear, Nose, Throat
Date received: 2023-02-07
Decision date: 2023-02-24
Decision: Unknown
Clearance type: Special
Location: New York, NY, US

Download summary PDF View on FDA.gov ↗

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K210137 — EsoCheck Cell Collection Device2021-02-18

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