BAXTER APD 12' EXTENSION LINE

BAXTER APD 12' EXTENSION LINE is an FDA 510(k)-cleared medical device (K925403) 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 21, 1994. Regulation: 8.