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Product codes
NRI
Product code NRI
Device name
Autoantibodies, Nuclear Pore Glycoprotein Gp210
Medical specialty
Immunology
Device class
2
Regulation number
866.5090
Review panel
IM
Implant
N
Life sustaining/supporting
N
GMP exempt
N
Third party review
Y
Summary malfunction reporting
Eligible
Definition
The device is used for the detection, in human serum or plasma, of autoantibodies to gp210 (nuclear pore glycoprotein gp210) as an aid in the diagnosis of primary biliary cirrhosis.
Source
FDA openFDA device classification dataset
Related 510(k) Records
#
510(k), Device, Applicant table
510(k)
Device
Applicant
Decision date
K061842
QUANTA LITE PBC SCREEN IGG/IGA ELISA
Inova Diagnostics, Inc.
2006-10-18
K040885
QUANTA LITE GP210 ELISA
Inova Diagnostics, Inc.
2004-06-25
Related GUDID Devices
#
Primary DI, Brand, Company table
Primary DI
Brand
Company
Published
04049016124887
EUROLINE Profile Autoimmune Liver Disease 8 Ag (IgG)
EUROIMMUN Medizinische Labordiagnostika AG
2016-09-24
04049016124894
EUROLINE Profile Autoimmune Liver Disease 8 Ag (IgG)
EUROIMMUN Medizinische Labordiagnostika AG
2016-09-24
08426950594239
QUANTA LiteĀ® PBC Screen IgG/IgA ELISA
INOVA DIAGNOSTICS, INC.
2016-08-31
08426950595007
QUANTA LiteĀ® gp210 ELISA
INOVA DIAGNOSTICS, INC.
2016-08-31