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510(k) Data Aggregation

    K Number
    K240410
    Device Name
    EVOLVE Nitric Oxide Delivery System
    Manufacturer
    Malinckrodt Manufacturing LLC
    Date Cleared
    2024-05-28

    (106 days)

    Product Code
    MRN, MRP, MRQ
    Regulation Number
    868.5165
    Why did this record match?
    Applicant Name (Manufacturer) :

    Malinckrodt Manufacturing LLC

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    The Evolve DS must only be used in accordance with the indications, contraindications, warnings and precautions described in the nitric oxide drug packaging inserts and labeling and is indicated for use in term and near-term (>34weeks gestation) neonates with hypoxic respiratory failure associated with clinical or echocardiographic evidence of pulmonary hypertension. The Evolve DS is indicated for a maximum of 14 days use. The primary targeted clinical setting is the Neonatal Intensive Care Unit (NICU), and secondary targeted clinical setting is the transport of neonates.
    Device Description
    The EVOLVE Nitric Oxide (NO) Delivery System (DS) is used for administration and monitoring of INOMAX (nitric oxide for inhalation). It is comprised of a main delivery device (EVOLVE), an electronic blender (eINOblender) for backup use, and a Cart which holds the EVOLVE as well as INOMAX drug cylinders, an oxygen cylinder and miscellaneous parts.
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