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

    CHICK/REISON PATIENT EMERG. TROLLEY

    K Number: K834478 · Decision Feb 21, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    30
    Registration Numbers
    30
    Same Product Code
    30
    Applicant Total
    9
    Review Days
    63

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    Basic Information

    Device Name
    CHICK/REISON PATIENT EMERG. TROLLEY
    K Number
    K834478
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1980
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Professional Medical Products, Inc.
    Date Received
    December 20, 1983
    Decision Date
    February 21, 1984
    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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