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.. 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
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- New York, NY, US
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