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

    DC SERIES FLUID WARMING CABINET, DC SERIES FLUID WARMING CABINET

    K Number: K132202 · Decision Dec 6, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    71
    Registration Numbers
    71
    Same Product Code
    74
    Applicant Total
    4
    Review Days
    143

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    Basic Information

    Device Name
    DC SERIES FLUID WARMING CABINET, DC SERIES FLUID WARMING CABINET
    K Number
    K132202
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Enthermics Medical Systems, Inc.
    Date Received
    July 16, 2013
    Decision Date
    December 6, 2013
    Product Code
    LGZ
    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
    LGZ Warmer, Thermal, Infusion Fluid

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