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

    VARIAN MULTILEAF COLLIMATOR

    K Number: K893464 · Decision Aug 10, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    50
    Applicant Total
    86
    Review Days
    99

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    Basic Information

    Device Name
    VARIAN MULTILEAF COLLIMATOR
    K Number
    K893464
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.5710
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Varian Assoc., Inc.
    Date Received
    May 3, 1989
    Decision Date
    August 10, 1989
    Product Code
    IXI
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IXI Block, Beam-Shaping, Radiation Therapy

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