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

    SPIVE NEEDLE SYSTEM, MODIFICATION

    K Number: K904013 · Decision Oct 1, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    424
    Registration Numbers
    424
    Same Product Code
    1173
    Applicant Total
    1
    Review Days
    33

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    Basic Information

    Device Name
    SPIVE NEEDLE SYSTEM, MODIFICATION
    K Number
    K904013
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Pascall Medical Corp.
    Date Received
    August 29, 1990
    Decision Date
    October 1, 1990
    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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