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

    INVALIFT

    K Number: K910830 · Decision Jun 9, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    56
    Registration Numbers
    56
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    468

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    Basic Information

    Device Name
    INVALIFT
    K Number
    K910830
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6775
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    American Invalift Corp.
    Date Received
    February 27, 1991
    Decision Date
    June 9, 1992
    Product Code
    FRZ
    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
    FRZ Device, Patient Transfer, Powered

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