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Lateral Flow Immunochromatography Assay For Host Biomarkers Of Respiratory Infection

Page Type
Product Code
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.
Physical State
In vitro diagnostic device
Technical Method
Lateral flow immunochromatography
Target Area
Human clinical specimens
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3230
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QXA is linked to regulation 21CFR866.3230, which does not seem to exist yet. It may be pending at the moment.

Lateral Flow Immunochromatography Assay For Host Biomarkers Of Respiratory Infection

Page Type
Product Code
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.
Physical State
In vitro diagnostic device
Technical Method
Lateral flow immunochromatography
Target Area
Human clinical specimens
Regulation Medical Specialty
Microbiology
Review Panel
Microbiology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.3230
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QXA is linked to regulation 21CFR866.3230, which does not seem to exist yet. It may be pending at the moment.