www.fdanews.com/articles/191029-fda-clears-surmodics-sublime-sheath
FDA Clears SurModics’ Sublime Sheath
April 23, 2019
The FDA granted 510(k) clearance to SurModics’ Sublime guide sheath, a radial artery access device for use in coronary procedures.
Designed for kink resistance and strength, the flexible braid-reinforced device has a working length covered in hydrophilic coating, creating a lubricious surface. It includes a dilator and hemostasis valve with a side arm for flushing.
The device will be available in two lengths (120 and 150 centimeters) and two diameters (five and six French gage).