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

    PATIENT TURNING AND REPOSITIONING G DEV.

    K Number: K770499 · Decision Apr 29, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    244
    Registration Numbers
    244
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    46

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    Basic Information

    Device Name
    PATIENT TURNING AND REPOSITIONING G DEV.
    K Number
    K770499
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6785
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Patient Healthguards Corp.
    Date Received
    March 14, 1977
    Decision Date
    April 29, 1977
    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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