FDA 510(k)

ACUVUE (senofilcon C) Lente de Contacto Suave

N.º K: K160212 · 2016-03-28

SolicitanteJohnson & Johnson Vision Care, Inc.

Fecha de decisión2016-03-28

Código de productoLPL

Comité asesorOP

DecisiónSubstantially Equivalent

Resumen del dispositivo

ACUVUE (senofilcon C) Soft Contact Lens is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Vision Care, Inc.. It received FDA 510(k) clearance on 2016-03-28 under 510(k) number K160212. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the ACUVUE (senofilcon C) Soft Contact Lens?

ACUVUE (senofilcon C) Soft Contact Lens is a medical device that received FDA 510(k) clearance on 2016-03-28. The listed applicant is Johnson & Johnson Vision Care, Inc.. The 510(k) number is K160212.

When did ACUVUE (senofilcon C) Soft Contact Lens receive FDA 510(k) clearance?

ACUVUE (senofilcon C) Soft Contact Lens received FDA 510(k) clearance on 2016-03-28, under 510(k) number K160212.

Who is the listed applicant for ACUVUE (senofilcon C) Soft Contact Lens?

The FDA 510(k) record lists Johnson & Johnson Vision Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACUVUE (senofilcon C) Soft Contact Lens?

The FDA product code for ACUVUE (senofilcon C) Soft Contact Lens is LPL.

Ensayos clínicos relacionados

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Otros registros que enlistan a Johnson & Johnson Vision Care, Inc. como solicitante

K210930ACUVUE® OASYS MAX 1-DAY Lentes de Contacto (senofilcon A)K200243ACUVUE (senofilcon A) Lente de Contacto Suave Multifocal K180299ACUVUE OASYS (senofilcon A) con Aditivo Fotocrómico

Dispositivos relacionados (Código: LPL)

Fuente oficial

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