
Teleflexmedical, Inc.
Free shipping on orders over $99 · 30-day returns
Teleflex Rusch SoftSimplastic Foley Catheters is an FDA 510(k)-cleared medical device (K212077) manufactured by Teleflexmedical, Inc.. 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 July 26, 2023. Regulation: 8.