INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA.

INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA. is an FDA 510(k)-cleared medical device (K900555) 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 May 1, 1990. Regulation: 8.