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

    MK 808 SERIES NASAL OXYGEN SAMPLER

    K Number: K822608 · Decision Oct 4, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    82
    Registration Numbers
    82
    Same Product Code
    120
    Applicant Total
    45
    Review Days
    35

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    Basic Information

    Device Name
    MK 808 SERIES NASAL OXYGEN SAMPLER
    K Number
    K822608
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.1720
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Instrumentation Industries, Inc.
    Date Received
    August 30, 1982
    Decision Date
    October 4, 1982
    Product Code
    CCL
    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
    CCL Analyzer, Gas, Oxygen, Gaseous-Phase

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