DEN230008
- 510(k) number
- DEN230008
- Device name
- DermaSensor
- Applicant
- Dermasensor, Inc. FL · US
- Product code
- QZS — Software-Aided Adjunctive Diagnostic Device For Use
- Decision date
- 2024-01-12
- Date received
- 2023-02-02
- Decision
- Unknown
- Clearance type
- Direct
- Advisory committee
- General, Plastic Surgery
Official FDA record: DEN230008
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.