SONOLINE 7XX DIAGNOSTIC ULTRASOUND SYSTEM

SONOLINE 7XX DIAGNOSTIC ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K992046) 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 August 12, 1999. Regulation: 8.