BUNN MODEL #40 LOW PRESSURE ALARM

BUNN MODEL #40 LOW PRESSURE ALARM is an FDA 510(k)-cleared medical device (K790370) manufactured by The John Bunn Co.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 27, 1979. Regulation: 8.