BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

    GEBDI TRIBOS 501

    K Number: K092231 · Decision Nov 24, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    99
    Registration Numbers
    99
    Same Product Code
    54
    Applicant Total
    1
    Review Days
    124

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    Basic Information

    Device Name
    GEBDI TRIBOS 501
    K Number
    K092231
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3590
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Gebdi Dental-Products GmbH
    Date Received
    July 23, 2009
    Decision Date
    November 24, 2009
    Product Code
    ELM
    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
    ELM Denture, Plastic, Teeth

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