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

    DRUALIFT 500

    K Number: K801933 · Decision Aug 27, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    58
    Registration Numbers
    58
    Same Product Code
    20
    Applicant Total
    2
    Review Days
    15

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    Basic Information

    Device Name
    DRUALIFT 500
    K Number
    K801933
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5500
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Independent Transfer Equipment Co.
    Date Received
    August 12, 1980
    Decision Date
    August 27, 1980
    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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