BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

    HUMAN BETA-2 MICROGLOBULIN URINE KIT FOR USE ON THE SPAPLUS

    K Number: K122066 · Decision Aug 30, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    34
    Registration Numbers
    34
    Same Product Code
    52
    Applicant Total
    43
    Review Days
    45

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    Basic Information

    Device Name
    HUMAN BETA-2 MICROGLOBULIN URINE KIT FOR USE ON THE SPAPLUS
    K Number
    K122066
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    866.5630
    Medical Specialty
    Immunology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    The Binding Site Group , Ltd.
    Date Received
    July 16, 2012
    Decision Date
    August 30, 2012
    Product Code
    JZG
    Advisory Committee
    Immunology
    Review Advisory Committee
    IM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    JZG System, Test, Beta-2-Microglobulin Immunological

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