BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇰 Denmark

    SCANLISA HUMAN CRP ELISA KIT

    K Number: K894573 · Decision Aug 10, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    46
    Registration Numbers
    46
    Same Product Code
    125
    Applicant Total
    1
    Review Days
    20

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    Basic Information

    Device Name
    SCANLISA HUMAN CRP ELISA KIT
    K Number
    K894573
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.5270
    Medical Specialty
    Immunology
    Decision
    Substantially Equivalent
    Applicant
    Immuntech A/S
    Date Received
    July 21, 1989
    Decision Date
    August 10, 1989
    Product Code
    DCK
    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
    DCK C-Reactive Protein, Antigen, Antiserum, And Control

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