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

    MANAN HUBER STYLE INFUSION NEEDLE

    K Number: K883744 · Decision Sep 28, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    39
    Review Days
    27

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    Basic Information

    Device Name
    MANAN HUBER STYLE INFUSION NEEDLE
    K Number
    K883744
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Manan Medical Products, Inc.
    Date Received
    September 1, 1988
    Decision Date
    September 28, 1988
    Product Code
    FMF
    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
    FMF Syringe, Piston

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