BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇮🇹 Italy

    ATR 5000, LC 5000, IMPLANT SYSTEM

    K Number: K033597 · Decision Nov 25, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    88
    Registration Numbers
    88
    Same Product Code
    88
    Applicant Total
    2
    Review Days
    11

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    Basic Information

    Device Name
    ATR 5000, LC 5000, IMPLANT SYSTEM
    K Number
    K033597
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4200
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Advanced Technology Research (A.T.R.) S.R.L.
    Date Received
    November 14, 2003
    Decision Date
    November 25, 2003
    Product Code
    EKX
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    Y

    Classifications

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

    Product Code Device Name
    EKX Handpiece, Direct Drive, Ac-Powered

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