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FDA 510(k), K123999, ILLUMASK ACNE LIGHT THERAPY MASK
FDA 510(k), K123999, ILLUMASK ACNE LIGHT THERAPY MASK
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$149.00 USD
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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
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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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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