BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

    EVACU SLED

    K Number: K913520 · Decision Dec 4, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    124
    Registration Numbers
    124
    Same Product Code
    38
    Applicant Total
    1
    Review Days
    119

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    Basic Information

    Device Name
    EVACU SLED
    K Number
    K913520
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6900
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Nexus Health Care Products , Ltd.
    Date Received
    August 7, 1991
    Decision Date
    December 4, 1991
    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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