BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    SOLUTION ADMINISTRATION SET (#2C0631)

    K Number: K760505 · Decision Sep 3, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    83
    Registration Numbers
    83
    Same Product Code
    34
    Applicant Total
    206
    Review Days
    11

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    Basic Information

    Device Name
    SOLUTION ADMINISTRATION SET (#2C0631)
    K Number
    K760505
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5420
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Travenol Laboratories, S.A.
    Date Received
    August 23, 1976
    Decision Date
    September 3, 1976
    Product Code
    KZD
    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
    KZD Infusor, Pressure, For I.V. Bags

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