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The Ventricular Catheter Set is used to obtain access to a ventricular cavity of the brain to drain fluid externally for the purpose of relieving elevated intracranial pressure or fluid volume.

The Ventricular Catheter Set is used to obtain access to a ventricular cavity of the brain to drain fluid externally for the purpose of relieving elevated intracranial pressure or fluid volume. The device is supplied sterile and is intended for one-time use. The materials comprising the device have an established history of use in medical product manufacturing.

This document (K962097) is a 510(k) summary for a Ventricular Catheter Set. It describes the device, its intended use, and its substantial equivalence to predicate devices.

However, a crucial piece of information is missing: the entire section outlining the acceptance criteria and the study proving the device meets those criteria. The provided text only includes the administrative and descriptive parts of the 510(k) summary.

Therefore, I cannot provide the requested information in the format specified because the core information about testing, acceptance criteria, and study details is not present in the provided snippet.

To answer your request, I would need a section of the 510(k) summary that details:

• Performance testing conducted (e.g., mechanical testing, biocompatibility, sterility, flow rates).
• Specific acceptance criteria for each test.
• Results from those tests.
• Protocols for how those results were obtained.

Without that, I can only state what the document does provide, which is not what you asked for regarding acceptance criteria and study details.

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