5 MHZ ADULT/PEDI TRANSESOPHAGEAL ECHO(TEE) TRANSDU

5 MHZ ADULT/PEDI TRANSESOPHAGEAL ECHO(TEE) TRANSDU is an FDA 510(k)-cleared medical device (K910669) manufactured by Siemens Ultrasound, 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 March 14, 1991. Regulation: 8.