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

    MAXIFILL TRANSFER SET

    K Number: K842345 · Decision Aug 17, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    177
    Registration Numbers
    177
    Same Product Code
    205
    Applicant Total
    8
    Review Days
    64

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    Basic Information

    Device Name
    MAXIFILL TRANSFER SET
    K Number
    K842345
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Lyphomed, Inc.
    Date Received
    June 14, 1984
    Decision Date
    August 17, 1984
    Product Code
    LHI
    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
    LHI Set, I.V. Fluid Transfer

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    Other Clearances by Lyphomed, Inc.

    K Number Device Name
    K910142 SPARK KIT(R), MODIFICATION
    K864509 SPARK-KIT(TM)
    K853019 NITROGLYCERIN INFUSION SET
    K853086 SECONDARY ADMINISTRATION SET
    K852881 VENTED SECONDARY IV ADMINISTRATION SET
    K852882 MAXIFILL TRANSFER SET
    K842678 I.V. TRANSFER SPIKE