KUDO (POWERED ROTATION BED)

KUDO (POWERED ROTATION BED) is an FDA 510(k)-cleared medical device (K905390) manufactured by Kinetic Concepts, Inc.. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 7, 1991. Regulation: 8.