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

    REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100

    K Number: K874639 · Decision Dec 4, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    30
    Registration Numbers
    30
    Same Product Code
    30
    Applicant Total
    23
    Review Days
    22

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    Basic Information

    Device Name
    REMOTE-CONTROLLED UNIVERSAL DIAG. TABLE RS-100
    K Number
    K874639
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1980
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Shimadzu Precision Instruments, Inc.
    Date Received
    November 12, 1987
    Decision Date
    December 4, 1987
    Product Code
    KXJ
    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
    KXJ Table, Radiologic

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