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FDA 510(k)

Neutrogena Light Therapy Aging Mask+

K-Number: K180856 · 2018-06-19

ApplicantJohnson & Johnson Consumer, Inc.
Decision Date2018-06-19
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Neutrogena Light Therapy Aging Mask+ is a medical device manufactured by Johnson & Johnson Consumer, Inc.. It received FDA 510(k) clearance on 2018-06-19 under approval number K180856. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Neutrogena Light Therapy Aging Mask+?

Neutrogena Light Therapy Aging 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 K180856.

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

Neutrogena Light Therapy Aging Mask+ received FDA 510(k) clearance on 2018-06-19, under approval number K180856.

What company makes Neutrogena Light Therapy Aging Mask+?

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

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

The FDA product code for Neutrogena Light Therapy Aging Mask+ is OHS.

Related Clinical Trials

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Related PubMed Literature

PMID: 40417352 Regulatory aspects of optogenetic research and therapy for retinitis pigmentosa under EU law. Frontiers in medical technology (2025)

Other Devices by Johnson & Johnson Consumer, Inc.

K180847Neutrogena Light Therapy Acne Mask+

Related Devices (Code: OHS)

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Official Source

View on FDA Database →

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

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