SERAFLO ARTERIAL AND VENOUS BLOODLINE SETS

SERAFLO ARTERIAL AND VENOUS BLOODLINE SETS is an FDA 510(k)-cleared medical device (K913526) manufactured by Althin Medical AB an Affiliate of Baxter Intl. 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 October 31, 1991. Regulation: 8.