LIGHTHOUSE URINARY CATHETER

LIGHTHOUSE URINARY CATHETER is an FDA 510(k)-cleared medical device (K140099) manufactured by Seedings Life Science Ventures, LLC. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 3, 2014. Regulation: 8.