BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    CORDIA A

    K Number: K810046 · Decision Feb 25, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    17
    Applicant Total
    315
    Review Days
    44

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    Basic Information

    Device Name
    CORDIA A
    K Number
    K810046
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3220
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Cordis Corp.
    Date Received
    January 12, 1981
    Decision Date
    February 25, 1981
    Product Code
    KHW
    Advisory Committee
    Microbiology
    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
    KHW Antigen, Id, Ha, Cep, Entamoeba Histolytica & Rel. Spp.

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