← FDA Medical Device Classifications

Immunohistochemistry Assay, Antibody, Programmed Death-Ligand 1

PLS · Class III — High Risk (PMA approval required, life-sustaining) · Unknown

Classification

FDA Product Code
PLS
Device class
Class III — High Risk (PMA approval required, life-sustaining)
Regulation
Review panel
PA
Medical specialty
Unknown
Submission type
2
GMP exempt
N
Life sustaining
N
Implant
N
Third-party review
N

Definition

The programmed death-ligand 1 (PD-L1) antibody is a qualitative immunohistochemical antibody intended to identify PD-L1 protein expression in human clinical tissue specimens. The PD-L1 antibody is indicated as an aid in identifying patients eligible for treatment with specific FDA approved therapeutic drugs or to assess PD-L1 expression level in patients who may respond particularly well to specific FDA approved therapeutic drugs.

Market data

Cleared 510(k) submissions
0
Registered establishments
4

Source

Authoritative
FDA Device Classification database
Machine
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