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

    A.C. POWER PATIENT LIFT

    K Number: K935351 · Decision Feb 28, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    58
    Registration Numbers
    58
    Same Product Code
    20
    Applicant Total
    2
    Review Days
    115

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    Basic Information

    Device Name
    A.C. POWER PATIENT LIFT
    K Number
    K935351
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5500
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Ken Kemmerer
    Date Received
    November 5, 1993
    Decision Date
    February 28, 1994
    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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