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FDA 510(k)

Neutrogena Light Therapy Acne Mask+

K-Number: K180847 · 2018-06-19

Decision Date2018-06-19
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Neutrogena Light Therapy Acne Mask+ is a medical device manufactured by Johnson & Johnson Consumer, Inc.. It received FDA 510(k) clearance on 2018-06-19 under approval number K180847. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Neutrogena Light Therapy Acne Mask+?

Neutrogena Light Therapy Acne Mask+ is a medical device that received FDA 510(k) clearance on 2018-06-19. It is manufactured by Johnson & Johnson Consumer, Inc.. The 510(k) number is K180847.

When was Neutrogena Light Therapy Acne Mask+ approved by the FDA?

Neutrogena Light Therapy Acne Mask+ received FDA 510(k) clearance on 2018-06-19, under approval number K180847.

What company makes Neutrogena Light Therapy Acne Mask+?

Neutrogena Light Therapy Acne Mask+ is manufactured by Johnson & Johnson Consumer, Inc..

What is the FDA product code for Neutrogena Light Therapy Acne Mask+?

The FDA product code for Neutrogena Light Therapy Acne Mask+ is OLP.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.