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

    HARE EMERGENCY STRETCHER

    K Number: K900670 · Decision Apr 23, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    124
    Registration Numbers
    124
    Same Product Code
    38
    Applicant Total
    5
    Review Days
    69

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    Basic Information

    Device Name
    HARE EMERGENCY STRETCHER
    K Number
    K900670
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6900
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Dyna Corp.
    Date Received
    February 13, 1990
    Decision Date
    April 23, 1990
    Product Code
    FPP
    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
    FPP Stretcher, Hand-Carried

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