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

    MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02

    K Number: K023293 · Decision Dec 23, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    123
    Registration Numbers
    124
    Same Product Code
    717
    Applicant Total
    8
    Review Days
    82

    Basic Information

    Device Name
    MED-TEC BELLYBOARD, MODELS MT-BBA-01 & MT-BBA-02
    K Number
    K023293
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.5050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    MED-TEC,INC.
    Date Received
    October 2, 2002
    Decision Date
    December 23, 2002
    Product Code
    IYE
    Advisory Committee
    Radiology
    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
    IYE Accelerator, Linear, Medical

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