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

    IN EXAM INTRAORAL DENTAL X-RAY SYSTEM

    K Number: K050019 · Decision Jan 31, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    60
    Registration Numbers
    60
    Same Product Code
    189
    Applicant Total
    20
    Review Days
    26

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    Basic Information

    Device Name
    IN EXAM INTRAORAL DENTAL X-RAY SYSTEM
    K Number
    K050019
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.1800
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Kavo America
    Date Received
    January 5, 2005
    Decision Date
    January 31, 2005
    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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