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

    SOLOLIFT - PATIENT TRANSFER STRETCHER

    K Number: K871475 · Decision May 11, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    244
    Registration Numbers
    244
    Same Product Code
    4
    Applicant Total
    8
    Review Days
    27

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    Basic Information

    Device Name
    SOLOLIFT - PATIENT TRANSFER STRETCHER
    K Number
    K871475
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6785
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Adel Medical , Ltd.
    Date Received
    April 14, 1987
    Decision Date
    May 11, 1987
    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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