Nutra Light Advanced

FDA 510(k) K150370 · Nutra Luxe MD, LLC

Substantially Equivalent

510(k) numberK150370

Submission

Device name
Nutra Light Advanced
Applicant
Nutra Luxe MD, LLC
Fort Myers, FL, US
Received
February 13, 2015
Decision date
July 22, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OLP – Over-The-Counter Powered Light Based Laser For Acne
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4810
Specialty
General, Plastic Surgery

The device is intended for over-the-counter (otc) use to treat patients with mild to moderate acne vulgaris. The device is intended to emit energy in the red and blue region of the spectrum, specifically indicated to treat mild to moderate acne vulgaris.

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K141596Nutra Stim Hair Laser CombOAP · Traditional 01/08/2015SE
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K141308Nutra Light RedOHS · Traditional 08/20/2014SE
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Questions and answers

When was Nutra Light Advanced cleared by the FDA?

Nutra Light Advanced (K150370) received a 510(k) decision of Substantially Equivalent on July 22, 2015, 159 days after the submission was received.

What is the product code of K150370?

The FDA product code is OLP – Over-The-Counter Powered Light Based Laser For Acne, a Class II (moderate risk) device regulated under 21 CFR 878.4810.