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

    DIAGNODENT 2190 WITH PERIODONTAL PROBE

    K Number: K060080 · Decision Feb 8, 2006
    View on FDA
    Classifications
    1
    FEI Numbers
    23
    Registration Numbers
    23
    Same Product Code
    10
    Applicant Total
    1
    Review Days
    29

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    Basic Information

    Device Name
    DIAGNODENT 2190 WITH PERIODONTAL PROBE
    K Number
    K060080
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    872.1745
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Kavo Dental Corporation
    Date Received
    January 10, 2006
    Decision Date
    February 8, 2006
    Product Code
    NTK
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    NTK Caries Detector, Laser Light, Transmission

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