Sonosite PX Ultrasound System

Sonosite PX Ultrasound System is an FDA 510(k)-cleared medical device (K200964) 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 May 7, 2020. Regulation: 8.