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

    HAUSTED POWERTRAN SERIES STRETCHER

    K Number: K041924 · Decision Sep 9, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    19
    Registration Numbers
    19
    Same Product Code
    11
    Applicant Total
    204
    Review Days
    55

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    Basic Information

    Device Name
    HAUSTED POWERTRAN SERIES STRETCHER
    K Number
    K041924
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.3690
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    STERIS Corporation
    Date Received
    July 16, 2004
    Decision Date
    September 9, 2004
    Product Code
    INK
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    INK Stretcher, Wheeled, Powered

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