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

    CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I

    K Number: K854562 · Decision Jan 9, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28
    Same Product Code
    29
    Applicant Total
    15
    Review Days
    56

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    Basic Information

    Device Name
    CONNECTOR, BLOOD TUBING, INFUSION T. INTRAVENOUS I
    K Number
    K854562
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Medelec Intl. Corp.
    Date Received
    November 14, 1985
    Decision Date
    January 9, 1986
    Product Code
    BRZ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    BRZ Set, Blood Transfusion

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