FDA 510(k), K123999, ILLUMASK ACNE LIGHT THERAPY MASK

FDA 510(k), K123999, ILLUMASK ACNE LIGHT THERAPY MASK

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510(K) Number: K123999
Device Name: ILLUMASK ACNE LIGHT THERAPY MASK
Manufacturer: LA LUMIERE, LLC
Device Classification Name: over-the-counter powered light based laser for acne
Regulation Number: 878.4810
Classification Product Code: OLP
Date Received: 12/26/2012
Decision Date: 08/28/2013
Regulation Medical Specialty: General & Plastic Surgery

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