Rusch Intermittent Urethral Catheters

Rusch Intermittent Urethral Catheters is an FDA 510(k)-cleared medical device (K222279) manufactured by Teleflex Medical. 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 August 28, 2022. Regulation: 8.