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

    PO-200 BLOOD OXYGEN MONITOR

    K Number: K811836 · Decision Jul 27, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18
    Same Product Code
    46
    Applicant Total
    2
    Review Days
    27

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    Basic Information

    Device Name
    PO-200 BLOOD OXYGEN MONITOR
    K Number
    K811836
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.2500
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Sumitomo Electric Industries, Inc.
    Date Received
    June 30, 1981
    Decision Date
    July 27, 1981
    Product Code
    KLK
    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
    KLK Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia

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    Other Clearances by Sumitomo Electric Industries, Inc.

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