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

    APPOLLO BATH

    K Number: K882669 · Decision Jul 8, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    35
    Applicant Total
    7
    Review Days
    11

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    Basic Information

    Device Name
    APPOLLO BATH
    K Number
    K882669
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.5150
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Electric Mobility, LLC
    Date Received
    June 27, 1988
    Decision Date
    July 8, 1988
    Product Code
    ILK
    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
    ILK Transport, Patient, Powered

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