EsoCheck Cell Collection Device— 510(k) K210137

Unknown

Lucid Diagnostics, Inc.

FDA 510(k) clearance K210137 for EsoCheck Cell Collection Device, Unknown on 2021-02-18. Applicant: Lucid Diagnostics, Inc..

Clearance details

Applicant: Lucid Diagnostics, Inc.
Product code: Code EOX
Advisory panel: Ear, Nose, Throat
Date received: 2021-01-19
Decision date: 2021-02-18
Decision: Unknown
Clearance type: Special
Location: New York, NY, US

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