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

    ANTI NEEDLE STRIKE ANTI DRUG ABUSE HYPO. SYRINGE

    K Number: K871007 · Decision Apr 30, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    5
    Review Days
    48

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    Basic Information

    Device Name
    ANTI NEEDLE STRIKE ANTI DRUG ABUSE HYPO. SYRINGE
    K Number
    K871007
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Habley Medical Technology Corp.
    Date Received
    March 13, 1987
    Decision Date
    April 30, 1987
    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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