ACUSON S1000 / S2000 / S3000

ACUSON S1000 / S2000 / S3000 is an FDA 510(k)-cleared medical device (K132804) manufactured by Siemens Medical Solutions USA, Inc. Ultrasound Gro. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 23, 2013. Regulation: 8.