UltraVision 2 Diagnostic Ultrasound System

UltraVision 2 Diagnostic Ultrasound System is an FDA 510(k)-cleared medical device (K173265) manufactured by Winprobe Corporation. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 6, 2017. Regulation: 8.