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

    ORTHOPHOS XG DS/CEPH

    K Number: K033073 · Decision Oct 10, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    60
    Registration Numbers
    60
    Same Product Code
    189
    Applicant Total
    42
    Review Days
    11

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    Basic Information

    Device Name
    ORTHOPHOS XG DS/CEPH
    K Number
    K033073
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    872.1800
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Sirona Dental Systems GmbH
    Date Received
    September 29, 2003
    Decision Date
    October 10, 2003
    Product Code
    EHD
    Advisory Committee
    Dental
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    EHD Unit, X-Ray, Extraoral With Timer

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