SONOLINE ELEGRA WITH SIESCAPE FEATURE

SONOLINE ELEGRA WITH SIESCAPE FEATURE is an FDA 510(k)-cleared medical device (K961833) 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 October 28, 1996. Regulation: 8.