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

    HOTLINE FLUID WARMER

    K Number: K911383 · Decision Oct 17, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    71
    Registration Numbers
    71
    Same Product Code
    74
    Applicant Total
    5
    Review Days
    203

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    Basic Information

    Device Name
    HOTLINE FLUID WARMER
    K Number
    K911383
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Level 1 Technologies, Inc.
    Date Received
    March 28, 1991
    Decision Date
    October 17, 1991
    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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    Other Clearances by Level 1 Technologies, Inc.

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