EsoCheck Cell Collection Device— 510(k) K222366

Unknown

Lucid Diagnostics, Inc.

FDA 510(k) clearance K222366 for EsoCheck Cell Collection Device, Unknown on 2022-10-26. Applicant: Lucid Diagnostics, Inc..

Clearance details

Applicant: Lucid Diagnostics, Inc.
Product code: Code EOX
Advisory panel: Ear, Nose, Throat
Date received: 2022-08-04
Decision date: 2022-10-26
Decision: Unknown
Clearance type: Traditional
Location: New York, NY, US

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