INTERSON ENDOCAVITY PROBE/ALOKA ULTRASOUND SYSTEM

INTERSON ENDOCAVITY PROBE/ALOKA ULTRASOUND SYSTEM is an FDA 510(k)-cleared medical device (K911114) manufactured by Interson 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 November 18, 1991. Regulation: 8.