FDA 510(k) K230076, Enhanced AURORA™ Medical Diode System, and related accessories, Psoria-Shield, Inc.
FDA 510(k) K230076, Enhanced AURORA™ Medical Diode System, and related accessories, Psoria-Shield, Inc.
Device Name: Enhanced AURORA™ Medical Diode System, and related accessories
Manufacturer: Psoria-Shield, Inc.
Device Classification Name: Light, Ultraviolet, Dermatological
Regulation Number: 878.4630
Classification Product Code: FTC
Date Received: 01/10/2023
Decision Date: 03/08/2023
Regulation Medical Specialty: General & Plastic Surgery
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