Neutrogena Light Therapy Aging Mask+
K-Number: K180856 · 2018-06-19
Device Summary
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. The listed applicant is Johnson & Johnson Consumer, Inc.. The 510(k) number is K180856.
When did Neutrogena Light Therapy Aging Mask+ receive FDA 510(k) clearance?
Neutrogena Light Therapy Aging Mask+ received FDA 510(k) clearance on 2018-06-19, under 510(k) number K180856.
Who is the listed applicant for Neutrogena Light Therapy Aging Mask+?
The FDA 510(k) record lists Johnson & Johnson Consumer, Inc. as the applicant. This does not by itself establish the device manufacturer.
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
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Johnson & Johnson Consumer, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: OHS)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.