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

    NEEDLE SYRINGE DISPOSAL DEVICE

    K Number: K896195 · Decision Nov 27, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    92
    Registration Numbers
    92
    Same Product Code
    112
    Applicant Total
    1
    Review Days
    33

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    Basic Information

    Device Name
    NEEDLE SYRINGE DISPOSAL DEVICE
    K Number
    K896195
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5570
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Advanced Medical Components, Inc.
    Date Received
    October 25, 1989
    Decision Date
    November 27, 1989
    Product Code
    MMK
    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
    MMK Container, Sharps

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