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FDA PMA

Immunohistochemistry assay, antibody, programmed death-ligand 1

PMA Number: P150013 · 2026-09-21

ApplicantAgilent Technologies, Inc.
Decision Date2026-09-21
PMA NumberP150013
Product CodePLS
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteePA

Device Summary

Immunohistochemistry assay, antibody, programmed death-ligand 1 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 2026-09-21. The device is classified under product code PLS. It was reviewed by the PA advisory panel.

Frequently Asked Questions

What is the Immunohistochemistry assay, antibody, programmed death-ligand 1?

Immunohistochemistry assay, antibody, programmed death-ligand 1 is a medical device that received FDA 510(k) clearance on 2026-09-21. The listed applicant is Agilent Technologies, Inc..

When did Immunohistochemistry assay, antibody, programmed death-ligand 1 receive FDA 510(k) clearance?

The clearance date for Immunohistochemistry assay, antibody, programmed death-ligand 1 can be found in the official FDA records.

Who is the listed applicant for Immunohistochemistry assay, antibody, programmed death-ligand 1?

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, programmed death-ligand 1?

The FDA product code for Immunohistochemistry assay, antibody, programmed death-ligand 1 is PLS.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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