Site-Rite Prevue Ultrasound System, Site-Rite Prevue+ Ultrasound System

Site-Rite Prevue Ultrasound System, Site-Rite Prevue+ Ultrasound System is an FDA 510(k)-cleared medical device (K150529) manufactured by C.R. Bard, 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 March 29, 2015. Regulation: 8.