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

    125I-IGE RADIOIMMUNOASSAY KIT

    K Number: K801019 · Decision May 20, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    30
    Registration Numbers
    30
    Same Product Code
    113
    Applicant Total
    2
    Review Days
    20

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    Basic Information

    Device Name
    125I-IGE RADIOIMMUNOASSAY KIT
    K Number
    K801019
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.5510
    Medical Specialty
    Immunology
    Decision
    Substantially Equivalent
    Applicant
    Bio-Ria
    Date Received
    April 30, 1980
    Decision Date
    May 20, 1980
    Product Code
    DGC
    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
    DGC Ige, Antigen, Antiserum, Control

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    Other Clearances by Bio-Ria

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    K812901 125I FERRITIN RADIOIMMUNOASSAY KIT