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

    OXYGEN SUPPLY TUBING

    K Number: K802071 · Decision Sep 16, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    230
    Registration Numbers
    230
    Same Product Code
    61
    Applicant Total
    1
    Review Days
    20

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    Basic Information

    Device Name
    OXYGEN SUPPLY TUBING
    K Number
    K802071
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.5860
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Auburn Components
    Date Received
    August 27, 1980
    Decision Date
    September 16, 1980
    Product Code
    BYX
    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
    BYX Tubing, Pressure And Accessories

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