FDA product code QGN

Lateral Flow Immunochromatography Assay For Host Infection Biomarkers

Microbiology·Class 2·21 CFR 866.3230
US regulatory classifications
US Product Code (FDA)
QGN
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US Risk Class (FDA)
Class 2
US Regulation (CFR)
21 CFR 866.3230
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Medical specialty
Microbiology
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Not Eligible
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.

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About this record

Lateral Flow Immunochromatography Assay For Host Infection Biomarkers is a medical device type in the Microbiology specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.