SLEEP I/T-5 AND SLEEP I/T-8

SLEEP I/T-5 AND SLEEP I/T-8 is an FDA 510(k)-cleared medical device (K904432) manufactured by Cns, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 9, 1991. Regulation: 8.