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

    CRITERION 60 OR PM 60

    K Number: K000959 · Decision Jun 22, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    55
    Registration Numbers
    55
    Same Product Code
    77
    Applicant Total
    5
    Review Days
    90

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    Basic Information

    Device Name
    CRITERION 60 OR PM 60
    K Number
    K000959
    Device Class
    FDA class 2
    Clearance Type
    Abbreviated
    Regulation Number
    868.2600
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Caradyne, Ltd.
    Date Received
    March 24, 2000
    Decision Date
    June 22, 2000
    Product Code
    CAP
    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
    CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

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