BOEHRINGER AUTOVAC(R) 7900 SERIES

BOEHRINGER AUTOVAC(R) 7900 SERIES is an FDA 510(k)-cleared medical device (K945775) 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 October 18, 1995. Regulation: 8.