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

    THYMUNE-T

    K Number: K780874 · Decision Jun 14, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    12
    Applicant Total
    17
    Review Days
    15

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    Basic Information

    Device Name
    THYMUNE-T
    K Number
    K780874
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.5870
    Medical Specialty
    Immunology
    Decision
    Substantially Equivalent
    Applicant
    Burroughs Wellcome Co.
    Date Received
    May 30, 1978
    Decision Date
    June 14, 1978
    Product Code
    DDC
    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
    DDC Thyroglobulin, Antigen, Antiserum, Control

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