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PMA de la FDA

Immunohistochemistry assay, antibody, epidermal growth factor receptor

Número de PMA: P030044 · 2019-03-13

SolicitanteAgilent Technologies, Inc.
Fecha de decisión2019-03-13
Número PMAP030044
Código de productoNQF
Clase del dispositivoClase 3
Especialidad médicaH
Número de regulación21 CFR 8
Comité asesorPA

Resumen del dispositivo

Immunohistochemistry assay, antibody, epidermal growth factor receptor is the device name listed in this FDA 510(k) record. The listed applicant is Agilent Technologies, Inc.. It received FDA 510(k) clearance on 2019-03-13. The device is classified under product code NQF. It was reviewed by the PA advisory panel.

Preguntas frecuentes

What is the Immunohistochemistry assay, antibody, epidermal growth factor receptor?

Immunohistochemistry assay, antibody, epidermal growth factor receptor is a medical device that received FDA 510(k) clearance on 2019-03-13. The listed applicant is Agilent Technologies, Inc..

When did Immunohistochemistry assay, antibody, epidermal growth factor receptor receive FDA 510(k) clearance?

The clearance date for Immunohistochemistry assay, antibody, epidermal growth factor receptor can be found in the official FDA records.

Who is the listed applicant for Immunohistochemistry assay, antibody, epidermal growth factor receptor?

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

What is the FDA product code for Immunohistochemistry assay, antibody, epidermal growth factor receptor?

The FDA product code for Immunohistochemistry assay, antibody, epidermal growth factor receptor is NQF.

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.

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