XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set

XABO Ventricular Catheter, XABO Peritoneal Catheter, XABO Catheter Set is an FDA 510(k)-cleared medical device (K242003) manufactured by Aesculap, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 15, 2024. Regulation: 8.