BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL

    K Number: K912696 · Decision Sep 16, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    34
    Registration Numbers
    34
    Same Product Code
    39
    Applicant Total
    23
    Review Days
    90

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    Basic Information

    Device Name
    TRAUMA VIEW RAD SYST MODEL #B-TRV/STRET MOBIL TABL
    K Number
    K912696
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    892.1770
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Bennett X-Ray Corp.
    Date Received
    June 18, 1991
    Decision Date
    September 16, 1991
    Product Code
    IYB
    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
    IYB Tube Mount, X-Ray, Diagnostic

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