AUTOWAND(TM) 7XXX SERIES

AUTOWAND(TM) 7XXX SERIES is an FDA 510(k)-cleared medical device (K902059) manufactured by Boehringer Laboratories. 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 23, 1990. Regulation: 8.