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

    MODIFICATION TO LTV 1000 VENTILATOR

    K Number: K040540 · Decision Apr 29, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    504
    Applicant Total
    12
    Review Days
    58

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    Basic Information

    Device Name
    MODIFICATION TO LTV 1000 VENTILATOR
    K Number
    K040540
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    868.5895
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Pulmonetic Systems, Inc.
    Date Received
    March 2, 2004
    Decision Date
    April 29, 2004
    Product Code
    CBK
    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
    CBK Ventilator, Continuous, Facility Use

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    Other Clearances by Pulmonetic Systems, Inc.

    K Number Device Name
    K083688 PULMONETIC SYSTEMS LTV 1200 MR CONDITIONAL VENTILATOR
    K070594 PALMTOP VENTILATOR, MODELS PTV-8, PTV-10
    K060647 LTV 1200 VENTILATOR
    K060549 AUTOMOBILE LIGHTER POWER CORD
    K051767 LTV 1000 VENTILATOR
    K040790 MODIFICATION TO LTV 1000 VENTILATOR/BREATHING CIRCUITS
    K032226 LTV-1000 VENTILATOR
    K010608 MODIFICATION TO LAP TOP VENTILATOR (LTV)
    K002881 VENTILATOR, CONTINUOUS (RESPIRATOR), MODEL LTV 1000
    K984056 LTV 1000
    Search all 12 clearances from Pulmonetic Systems, Inc. →