AUTOVAC BP SYSTE, 2000 SERIES

AUTOVAC BP SYSTE, 2000 SERIES is an FDA 510(k)-cleared medical device (K955010) 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 June 19, 1996. Regulation: 8.