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

    COPPER KETTLE VAPORIZER PLUS

    K Number: K771150 · Decision Aug 4, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    56
    Applicant Total
    2
    Review Days
    38

    Basic Information

    Device Name
    COPPER KETTLE VAPORIZER PLUS
    K Number
    K771150
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5880
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    AIR PRODUCTS & CHEMICALS, INC.
    Date Received
    June 27, 1977
    Decision Date
    August 4, 1977
    Product Code
    CAD
    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
    CAD Vaporizer, Anesthesia, Non-Heated

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    Other Clearances by AIR PRODUCTS & CHEMICALS, INC.

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    K771134 ANESTHESIA BREATHING CIRCUIT