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

    KARECO INT'L WHEELCHAIR

    K Number: K843688 · Decision Nov 23, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    129
    Registration Numbers
    129
    Same Product Code
    458
    Applicant Total
    2
    Review Days
    65

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    Basic Information

    Device Name
    KARECO INT'L WHEELCHAIR
    K Number
    K843688
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.3850
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Kareco Intl., Inc.
    Date Received
    September 19, 1984
    Decision Date
    November 23, 1984
    Product Code
    IOR
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    IOR Wheelchair, Mechanical

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    Other Clearances by Kareco Intl., Inc.

    K Number Device Name
    K845031 KARECO INT'L - DOUGLE-HOOK I.V. STAND