ARTERIAL BLOOD TUBING SET FOR SINGLE NEEDLE HEMODIALYSIS

ARTERIAL BLOOD TUBING SET FOR SINGLE NEEDLE HEMODIALYSIS is an FDA 510(k)-cleared medical device (K955277) manufactured by Baxter Healthcare 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 February 15, 1996. Regulation: 8.