SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026

SANDHILL UNITIP CATHETER PRESSURE SENSOR, MODEL K 5251-L3-0026 is an FDA 510(k)-cleared medical device (K002427) manufactured by Sandhill Scientific, Inc.. 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 June 21, 2001. Regulation: 8.