BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    TENDERLIFT

    K Number: K800373 · Decision Mar 12, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    240
    Registration Numbers
    240
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    21

    Basic Information

    Device Name
    TENDERLIFT
    K Number
    K800373
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6785
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    COMPETENT DESIGN
    Date Received
    February 20, 1980
    Decision Date
    March 12, 1980
    Product Code
    FMR
    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
    FMR Device, Transfer, Patient, Manual

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