HF JUNIOR HEMOFILTER

HF JUNIOR HEMOFILTER is an FDA 510(k)-cleared medical device (K071298) manufactured by Minntech Corp.. 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 7, 2007. Regulation: 8.