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

    NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA

    K Number: K844578 · Decision May 14, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    105
    Registration Numbers
    105
    Same Product Code
    49
    Applicant Total
    10
    Review Days
    172

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    Basic Information

    Device Name
    NON-MAGNETIC EXAMINATION TABLE FOR MAGNETIC RESONA
    K Number
    K844578
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6910
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Engineering Dynamics Corp.
    Date Received
    November 23, 1984
    Decision Date
    May 14, 1985
    Product Code
    FPO
    Advisory Committee
    General Hospital
    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
    FPO Stretcher, Wheeled

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