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

    HOVERJACK AIR PATIENT LIFT DEVICE

    K Number: K041503 · Decision Aug 12, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    58
    Registration Numbers
    58
    Same Product Code
    20
    Applicant Total
    1
    Review Days
    66

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    Basic Information

    Device Name
    HOVERJACK AIR PATIENT LIFT DEVICE
    K Number
    K041503
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5500
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    D.T. Davis Enterprises , Ltd.
    Date Received
    June 7, 2004
    Decision Date
    August 12, 2004
    Product Code
    FNG
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FNG Lift, Patient, Ac-Powered

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