ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA

ALTERNATE BLOOD PORT DESIGN FOR ADDIT. MEMB. OF CA is an FDA 510(k)-cleared medical device (K882680) 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 July 21, 1988. Regulation: 8.