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

    QUICKIE P200

    K Number: K924278 · Decision Mar 28, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    125
    Registration Numbers
    125
    Same Product Code
    580
    Applicant Total
    6
    Review Days
    580

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    Basic Information

    Device Name
    QUICKIE P200
    K Number
    K924278
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.3860
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent for Some Indications
    Applicant
    Quickie Designs, Inc.
    Date Received
    August 25, 1992
    Decision Date
    March 28, 1994
    Product Code
    ITI
    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
    ITI Wheelchair, Powered

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    Other Clearances by Quickie Designs, Inc.

    K Number Device Name
    K972230 QUICKIE P90 SERIES
    K963381 QUICKIE P300 SERIES
    K963382 QUICKIE P100 SERIES
    K963385 QUICKIE POWER WHEELCHAIRS P200 SERIES
    K900330 QUICKIE P300 WHEELCHAIR