FDA 510(k), K103540, PSORIA-LIGHT

FDA 510(k), K103540, PSORIA-LIGHT

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510(K) Number: K103540
Device Name: PSORIA-LIGHT
Manufacturer: WAYNE GLOVER
Device Classification Name: Light, Ultraviolet, Dermatological
Regulation Number: FTC
Classification Product Code: 12/02/2010
Date Received: 02/10/2011
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery

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