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Siemens Medical Solutions USA, Inc., Ultrasound DI
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SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K072365) manufactured by Siemens Medical Solutions USA, Inc., Ultrasound DI. 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 16, 2007. Regulation: 8.