7250 ULTRASOUND IMAGING SYSTEM

7250 ULTRASOUND IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K982444) manufactured by Biosound Esaote, 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 5, 1998. Regulation: 8.