FDA 510(k)

Lentes de contacto suaves Alcon (serafilcon A) para uso diario

N.º K: K212806 · 2021-12-28

Fecha de decisión2021-12-28

Código de productoLPL

Comité asesorOP

DecisiónSubstantially Equivalent

Resumen del dispositivo

Alcon (serafilcon A) soft contact lenses for daily wear is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories, Inc.. It received FDA 510(k) clearance on 2021-12-28 under 510(k) number K212806. 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 Alcon (serafilcon A) soft contact lenses for daily wear?

Alcon (serafilcon A) soft contact lenses for daily wear is a medical device that received FDA 510(k) clearance on 2021-12-28. The listed applicant is Alcon Laboratories, Inc.. The 510(k) number is K212806.

When did Alcon (serafilcon A) soft contact lenses for daily wear receive FDA 510(k) clearance?

Alcon (serafilcon A) soft contact lenses for daily wear received FDA 510(k) clearance on 2021-12-28, under 510(k) number K212806.

Who is the listed applicant for Alcon (serafilcon A) soft contact lenses for daily wear?

The FDA 510(k) record lists Alcon Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Alcon (serafilcon A) soft contact lenses for daily wear?

The FDA product code for Alcon (serafilcon A) soft contact lenses for daily wear is LPL.

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Otros registros que enlistan a Alcon Laboratories, Inc. como solicitante

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Dispositivos relacionados (Código: LPL)

Fuente oficial

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