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

    TRANSCURE, MODEL 2910

    K Number: K022862 · Decision Oct 18, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    101
    Registration Numbers
    101
    Same Product Code
    213
    Applicant Total
    2
    Review Days
    51

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    Basic Information

    Device Name
    TRANSCURE, MODEL 2910
    K Number
    K022862
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.6070
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Kinetic Instruments, Inc.
    Date Received
    August 28, 2002
    Decision Date
    October 18, 2002
    Product Code
    EBZ
    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
    EBZ Activator, Ultraviolet, For Polymerization

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    Other Clearances by Kinetic Instruments, Inc.

    K Number Device Name
    K012946 SUNLITELED MODEL #2810