DermaSensor— 510(k) DEN230008

Unknown

Dermasensor, Inc.

FDA 510(k) clearance DEN230008 for DermaSensor, Unknown on 2024-01-12. Applicant: Dermasensor, Inc..

Clearance details

Applicant: Dermasensor, Inc.
Product code: Code QZS
Advisory panel: General, Plastic Surgery
Date received: 2023-02-02
Decision date: 2024-01-12
Decision: Unknown
Clearance type: Direct
Location: Miami, FL, US

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