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The Avanti + Catheter Sheath Introducer is indicated for use in arterial and venous procedures requiring percutaneous introduction of catheters and other intravascular devices.

As with other currently marketed Cordis CSIs mentioned in this submission, these devices provide vascular access for various intravascular devices through the valve while simultaneously maintaining hemostasis. Infusion of fluids into the vasculature and withdrawal of blood from the vasculature are possible using the sheath sideport.

I am sorry, but the provided text from the Preamble Notification 510(k) for the Cordis Corporation Avanti + Catheter Sheath Introducer (K970392) does not contain any information regarding specific acceptance criteria for device performance or any studies conducted to prove that the device meets such criteria.

The document primarily focuses on establishing substantial equivalence to predicate devices based on design, construction, and intended use, and mentions biocompatibility testing previously performed on the materials. It explicitly states that "Performance standards have not been established by the FDA under section 514 of the Food, Drug and Cosmetic Act."

Therefore, I cannot fulfill your request for the detailed table and study information because it is not present in the provided text.

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