FDA 510(k)

Neutrogena Light Therapy Acne Mask+

Número K: K180847 · 2018-06-19

RequerenteJohnson & Johnson Consumer, Inc.

Data da decisão2018-06-19

Código do produtoOLP

Comité consultivoSU

DecisãoSubstantially Equivalent

Resumo do dispositivo

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

Perguntas frequentes

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. The listed applicant is Johnson & Johnson Consumer, Inc.. The 510(k) number is K180847.

When did Neutrogena Light Therapy Acne Mask+ receive FDA 510(k) clearance?

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

Who is the listed applicant for Neutrogena Light Therapy Acne 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 Acne Mask+?

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

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Outros registros que listam Johnson & Johnson Consumer, Inc. como candidato(a)

K180856Neutrogena Light Therapy Aging Mask+

Dispositivos Relacionados (Código: OLP)

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Fonte oficial

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