DermaSensor— 510(k) DEN230008
UnknownDermasensor, Inc.
FDA 510(k) clearance DEN230008 for DermaSensor, Unknown on 2024-01-12. Applicant: Dermasensor, Inc.. Device class: 2.
Clearance details
- Applicant
- Dermasensor, Inc.
- Product code
- Code QZS
- Device class
- Class 2
- Regulation
- 21 CFR 878.1830
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Miami, FL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.