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U.S. Department of Health and Human Services

Product Classification

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Device autoantibodies, nuclear pore glycoprotein gp210
Regulation Description Antimitochondrial antibody immunological test system.
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.
Regulation Medical Specialty Immunology
Review Panel Immunology
Product CodeNRI
Premarket Review Office of In Vitro Diagnostics and Radiological Health (OIR)
Submission Type 510(k)
Regulation Number 866.5090
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Eligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review
Accredited Persons
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