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

    ZAP-IT!

    K Number: DEN100024 · Decision Nov 7, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    1
    Applicant Total
    1
    Review Days
    1520

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    Basic Information

    Device Name
    ZAP-IT!
    K Number
    DEN100024
    Device Class
    FDA class 2
    Clearance Type
    Post-NSE
    Regulation Number
    882.5894
    Medical Specialty
    Neurology
    Decision
    Unknown
    Applicant
    Ecobrands , Ltd.
    Date Received
    September 9, 2010
    Decision Date
    November 7, 2014
    Product Code
    OSG
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    OSG Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch

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