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

    ACCU-FLO REGULATOR

    K Number: K865077 · Decision Feb 10, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    111
    Registration Numbers
    112
    Same Product Code
    54
    Applicant Total
    1
    Review Days
    43

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    Basic Information

    Device Name
    ACCU-FLO REGULATOR
    K Number
    K865077
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.2700
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Alum-Ox, Inc.
    Date Received
    December 29, 1986
    Decision Date
    February 10, 1987
    Product Code
    CAN
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    CAN Regulator, Pressure, Gas Cylinder

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