BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇳🇴 Norway

    MOLIFT

    K Number: K851844 · Decision May 17, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    206
    Registration Numbers
    207
    Same Product Code
    12
    Applicant Total
    1
    Review Days
    21

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    Basic Information

    Device Name
    MOLIFT
    K Number
    K851844
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5510
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Madshus A/S
    Date Received
    April 26, 1985
    Decision Date
    May 17, 1985
    Product Code
    FSA
    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
    FSA Lift, Patient, Non-Ac-Powered

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