ACUSON S1000, S2000, S3000 DIAGNOSTIC ULTRASOUND SYSTEMS

ACUSON S1000, S2000, S3000 DIAGNOSTIC ULTRASOUND SYSTEMS is an FDA 510(k)-cleared medical device (K140959) manufactured by Siemens Medical Solutions USA, 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 April 29, 2014. Regulation: 8.