MEDLINE LATEX FOLEY CATHETER

MEDLINE LATEX FOLEY CATHETER is an FDA 510(k)-cleared medical device (K071423) manufactured by Medline Industries, 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 17, 2007. Regulation: 8.