TETRAD 2300 E/U ULTRASOUNG IMAGING SYSTEM

TETRAD 2300 E/U ULTRASOUNG IMAGING SYSTEM is an FDA 510(k)-cleared medical device (K946277) manufactured by Tetra Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 14, 1996. Regulation: 8.