BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇺 Australia

    V SET

    K Number: K900336 · Decision Oct 4, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    424
    Registration Numbers
    424
    Same Product Code
    1173
    Applicant Total
    11
    Review Days
    254

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    Basic Information

    Device Name
    V SET
    K Number
    K900336
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Go Medical Industries Pty. , Ltd.
    Date Received
    January 23, 1990
    Decision Date
    October 4, 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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    K890400 MODIFIED URINARY CATHETER INTRODUCER (UCI)
    K891465 OBSTETRIC CUP (MODIFICATION)
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