LIR · Antigen, Enzyme Linked Immunoabsorbent Assay, Neisseria Gonorrhoeae

Microbiology · 21 CFR 866.3390 · Class 2

Overview

Product CodeLIR
Device NameAntigen, Enzyme Linked Immunoabsorbent Assay, Neisseria Gonorrhoeae
Regulation21 CFR 866.3390
Device ClassClass 2
Review PanelMicrobiology
3rd-Party ReviewableYes

Identification

Neisseria spp. direct serological test reagents are devices that consist of antigens and antisera used in serological tests to identify Neisseria spp. from cultured isolates. Additionally, some of these reagents consist of Neisseria spp. antisera conjugated with a fluorescent dye (immunofluorescent reagents) which may be used to detect the presence of Neisseria spp. directly from clinical specimens. The identification aids in the diagnosis of disease caused by bacteria belonging to the genus Neisseria, such as epidemic cerebrospinal meningitis, meningococcal disease, and gonorrhea, and also provides epidemiological information on diseases caused by these microorganisms. The device does not include products for the detection of gonorrhea in humans by indirect methods, such as detection of antibodies or of oxidase produced by gonococcal organisms.

Classification Rationale

Class II (performance standards).

Recent Cleared Devices (3 of 3)

RecordDevice NameApplicantDecision DateDecision
K023947GC OIAThermo Biostar, Inc.Apr 17, 2003SESE
K882534ABBOTT TESTPACK(TM) GONORRHEA POSITIVE CONTROLAbbott LaboratoriesJul 12, 1988SESE
K881064HYGEIA GC TESTHygeia SciencesJun 2, 1988SESE

Top Applicants

Innolitics

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