BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED

BOEHRINGER LABORATORIES SUCTION REGULATOR, MODIFIED is an FDA 510(k)-cleared medical device (K933232) manufactured by Boehringer Laboratories. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 27, 1994. Regulation: 8.