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U.S. Department of Health and Human Services

Product Classification

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Device test system, antineutrophil cytoplasmic antibodies (anca)
Regulation Description Multiple autoantibodies immunological test system.
Regulation Medical Specialty Immunology
Review Panel Immunology
Product CodeMOB
Premarket Review Division of Immunology and Hematology Devices (DIHD)
Division of Immunology and Hematology Devices (DIHD)
Submission Type 510(k)
Regulation Number 866.5660
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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