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

    POLYFIN QR SUBCUTANEOUS INFUSION SET

    K Number: K954969 · Decision Feb 22, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    424
    Registration Numbers
    424
    Same Product Code
    1173
    Applicant Total
    48
    Review Days
    115

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    Basic Information

    Device Name
    POLYFIN QR SUBCUTANEOUS INFUSION SET
    K Number
    K954969
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medtronic Minimed
    Date Received
    October 30, 1995
    Decision Date
    February 22, 1996
    Product Code
    FPA
    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
    FPA Set, Administration, Intravascular

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