EsoCheck CCD Cell Collection Device— 510(k) K183262
UnknownLucid Diagnostics, Inc.
FDA 510(k) clearance K183262 for EsoCheck CCD Cell Collection Device, Unknown on 2019-06-21. Applicant: Lucid Diagnostics, Inc..
Clearance details
- Applicant
- Lucid Diagnostics, Inc.
- Product code
- Code EOX
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.