QXA — Lateral Flow Immunochromatography Assay For Host Biomarkers Of Respiratory Infection Class II

FDA Device Classification

Classification Details

Product Code
QXA
Device Class
Class II
Regulation Number
866.3230
Submission Type
Review Panel
MI
Medical Specialty
Microbiology
Implant
No

Definition

A device to detect and measure non-microbial analytes to aid in the detection and identification of localized human infections is identified as an in vitro device intended for the detection and qualitative measurement, quantitative measurement, or both of one or more non-microbial analytes in human clinical specimens to aid in the assessment, identification, or both of a localized microbial infection when used in conjunction with clinical signs and symptoms and other clinical and laboratory findings.

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K260787lumos diagnosticsFebriDx Bacterial/Non-bacterial AssayMarch 24, 2026
K230917lumos diagnosticsFebriDx Bacterial / Non-bacterial Point of Care AssayJune 30, 2023