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

    X-RAY POSITIONING DEVICE

    K Number: K770060 · Decision Jan 24, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    81
    Registration Numbers
    81
    Same Product Code
    355
    Applicant Total
    5
    Review Days
    13

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    Basic Information

    Device Name
    X-RAY POSITIONING DEVICE
    K Number
    K770060
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1680
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Robert R. Moore
    Date Received
    January 11, 1977
    Decision Date
    January 24, 1977
    Product Code
    KPR
    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
    KPR System, X-Ray, Stationary

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    Other Clearances by Robert R. Moore

    K Number Device Name
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    K770223 HEAVY FOAM HEEL & ELBOW PROTECTORS
    K770059 ORTHOPEDIC SPECIALTIES