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

    MDM ARTERIAL BLOOD GAS KIT

    K Number: K822786 · Decision Oct 21, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    39
    Registration Numbers
    39
    Same Product Code
    57
    Applicant Total
    7
    Review Days
    36

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    Basic Information

    Device Name
    MDM ARTERIAL BLOOD GAS KIT
    K Number
    K822786
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.1100
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Martell Medical Products, Inc.
    Date Received
    September 15, 1982
    Decision Date
    October 21, 1982
    Product Code
    CBT
    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
    CBT Arterial Blood Sampling Kit

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    Other Clearances by Martell Medical Products, Inc.

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