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

    BASE ONLY, TORONTO CHAIR

    K Number: K832322 · Decision Aug 12, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    23
    Applicant Total
    6
    Review Days
    28

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    Basic Information

    Device Name
    BASE ONLY, TORONTO CHAIR
    K Number
    K832322
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.3880
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Intl. Medical Equipment Corp.
    Date Received
    July 15, 1983
    Decision Date
    August 12, 1983
    Product Code
    IQC
    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
    IQC Wheelchair, Special Grade

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    K813104 POWER DRIVE WHEELCR
    K803307 MATTRESS, AIR FLOATATION, ALTERN. PRESS.