ACUSON S3000 S2000 S1000 Diagnostic Ultrasound Systems

ACUSON S3000 S2000 S1000 Diagnostic Ultrasound Systems is an FDA 510(k)-cleared medical device (K172162) manufactured by Siemens Healthcare. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 15, 2017. Regulation: 8.