BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇫🇷 France

    KODAK MODELS 2100 AND 2200

    K Number: K060292 · Decision Mar 3, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    60
    Registration Numbers
    60
    Same Product Code
    189
    Applicant Total
    1
    Review Days
    25

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    Basic Information

    Device Name
    KODAK MODELS 2100 AND 2200
    K Number
    K060292
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    872.1800
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Kodak-Trophy
    Date Received
    February 6, 2006
    Decision Date
    March 3, 2006
    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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