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

    MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS

    K Number: K013905 · Decision Apr 22, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    84
    Registration Numbers
    84
    Same Product Code
    160
    Applicant Total
    7
    Review Days
    147

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    Basic Information

    Device Name
    MODIFICATION EZ-1 SYSTEM REPIRATORY SENSORS
    K Number
    K013905
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    868.2375
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Pro-Tech Services, Inc.
    Date Received
    November 26, 2001
    Decision Date
    April 22, 2002
    Product Code
    MNR
    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
    MNR Ventilatory Effort Recorder

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