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PMA de la FDA

Immunohistochemistry test, DNA mismatch repair (MMR) Protein assay

Número de PMA: P250004 · 2026-09-11

SolicitanteAgilent Technologies, Inc.
Fecha de decisión2026-09-11
Número PMAP250004
Código de productoQNH
Clase del dispositivoClase 3
Especialidad médicaH
Número de regulación21 CFR 8
Comité asesorPA

Resumen del dispositivo

Immunohistochemistry test, DNA mismatch repair (MMR) Protein assay 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 2026-09-11. The device is classified under product code QNH. It was reviewed by the PA advisory panel.

Preguntas frecuentes

What is the Immunohistochemistry test, DNA mismatch repair (MMR) Protein assay?

Immunohistochemistry test, DNA mismatch repair (MMR) Protein assay is a medical device that received FDA 510(k) clearance on 2026-09-11. The listed applicant is Agilent Technologies, Inc..

When did Immunohistochemistry test, DNA mismatch repair (MMR) Protein assay receive FDA 510(k) clearance?

The clearance date for Immunohistochemistry test, DNA mismatch repair (MMR) Protein assay can be found in the official FDA records.

Who is the listed applicant for Immunohistochemistry test, DNA mismatch repair (MMR) Protein assay?

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 test, DNA mismatch repair (MMR) Protein assay?

The FDA product code for Immunohistochemistry test, DNA mismatch repair (MMR) Protein assay is QNH.

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Fuente oficial

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