Supplemental material for "Steady flow in a patient-averaged inferior vena cava - Part I: Particle Image Velocimetry Measurements at Rest and Exercise Conditions" (CVET)

ZIP archive containing PIV data and other supplemental material for:Gallagher, M. B., Aycock, K. I., Craven, B. A., and Manning K. B. Steady flow in a patient-averaged inferior vena cava - Part I: Particle Image Velocimetry Measurements at Rest and Exercise Conditions. <i>Cardiovascular Engineering and Technology. Accepted October 2018.</i>See also our companion paper:Craven, B. A., Aycock, K. I., and Manning, K. B. Steady flow in a patient-averaged inferior vena cava - Part II: Computational Fluid Dynamics Verification and Validation. <i>Cardiovascular Engineering and Technology. Accepted October 2018.</i>---<b>Tool Reference</b>RST Reference Number: RST24CV16.01Date of Publication: 09/24/2023Recommended Citation: U.S. Food and Drug Administration. (2023). <i>Benchmark Validation Dataset for Laminar Flow in an Anatomical Vascular Model of the Inferior Vena Cava</i> (RST24CV16.01). https://cdrh-rst.fda.gov/benchmark-validation-dataset-laminar-flow-anatomical-vascular-model-inferior-vena-cava<b>Disclaimer</b><b>About the Catalog of Regulatory Science Tools</b>The enclosed tool is part of the Catalog of Regulatory Science Tools, which provides a peer-reviewed resource for stakeholders to use where standards and qualified Medical Device Development Tools (MDDTs) do not yet exist. These tools do not replace FDA-recognized standards or MDDTs. This catalog collates a variety of regulatory science tools that the FDA's Center for Devices and Radiological Health's (CDRH) Office of Science and Engineering Labs (OSEL) developed. These tools use the most innovative science to support medical device development and patient access to safe and effective medical devices. If you are considering using a tool from this catalog in your marketing submissions, note that these tools have not been qualified as Medical Device Development Tools and the FDA has not evaluated the suitability of these tools within any specific context of use. You may request feedback or meetings for medical device submissions as part of the Q-Submission Program.For more information about the Catalog of Regulatory Science Tools, email [e-mail].