AMYSEAT TILT/RECLINE SEATING

AMYSEAT TILT/RECLINE SEATING is an FDA 510(k)-cleared medical device (K011006) manufactured by Amysystems. 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 May 10, 2001. Regulation: 8.