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510(k) Data Aggregation

    K Number
    K041321
    Date Cleared
    2004-07-09

    (52 days)

    Product Code
    Regulation Number
    884.1720
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The VEROSCOPE is used percutaneously for penetrating the abdominal cavity under endoscopic control to safely reach a defined body region. It therefore also serves to create a pneumoperitoneum under visual control in the abdomen.

    The Dilation Tube System and standard Dilation System is used for dilating surgically created passages in body cavities.

    Indications and field of use: The Veroscope and dilation tube systems are used for diagnosis and therapy in conjunction with endoscopic accessories in various disciplines such as surgery, gynecology and urology.

    Device Description

    The 'Veroscope' consists of an outer trocar sleeve with insufflation stopcock, a veress cannula rice + erosopo consisted brotection tube with a transparent blunt tip and an endoscope.

    The 'Veroscope' is similar to a spring-loaded, blunt Veress needle that is used for penetrating tissue layers under endoscopic view.

    The Standard Dilation System consists of metal dilation sleeves and a guide rod.

    The Dilation Tube System 4760 consists of a plastic dilation tube and trocars with sleeves of various dimensions.

    AI/ML Overview

    The provided document is a 510(k) Summary for a medical device (VEROSCOPE, Optical Veress Cannula and Dilation Tube System). It does not contain any information about acceptance criteria or a study proving the device meets acceptance criteria.

    The document explicitly states:

    • "No performance standards are known." (Section 5.0 Performance Data)
    • "No clinical tests performed." (Section 6.0 Clinical Tests)

    Therefore, based solely on the provided text, I cannot complete the requested table or provide information about a study proving acceptance criteria. The submission focuses on demonstrating substantial equivalence to predicate devices, not on presenting new performance data or clinical trial results for the device itself.

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