ACUSON S3000, S2000 Diagnostic Ultrasound System

ACUSON S3000, S2000 Diagnostic Ultrasound System is an FDA 510(k)-cleared medical device (K183575) manufactured by Siemens Healthineers. 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 19, 2019. Regulation: 8.