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510(k) Data Aggregation

    K Number
    K162951
    Device Name
    TUBETECH IV Administration Set
    Date Cleared
    2017-07-28

    (277 days)

    Product Code
    Regulation Number
    880.5440
    Why did this record match?
    Applicant Name (Manufacturer) :

    Douglas Medical Products, Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    For the administration of fluids from a container into the patient vascular system through a vascular access device.
    Device Description
    Not Found
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