FUJIFILM SonoSite X-Porte Ultrasound System

FUJIFILM SonoSite X-Porte Ultrasound System is an FDA 510(k)-cleared medical device (K152209) manufactured by FUJIFILM Sonosite, Inc.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 18, 2015. Regulation: 8.