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

    I.V. SET WITH IN-LINE FILTER

    K Number: K781785 · Decision Dec 7, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    424
    Registration Numbers
    424
    Same Product Code
    1173
    Applicant Total
    2
    Review Days
    50

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    Basic Information

    Device Name
    I.V. SET WITH IN-LINE FILTER
    K Number
    K781785
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Cutler Laboratories, Inc.
    Date Received
    October 18, 1978
    Decision Date
    December 7, 1978
    Product Code
    FPA
    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
    FPA Set, Administration, Intravascular

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