ACUSON S1000, S2000, S3000 Diagnostic Ultrasuond System

ACUSON S1000, S2000, S3000 Diagnostic Ultrasuond System is an FDA 510(k)-cleared medical device (K152369) manufactured by Siemens Medical Solutions USA, Inc. Ultrasound Group. 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 5, 2015. Regulation: 8.