REGULATOR, PRESSURE, CUFF

REGULATOR, PRESSURE, CUFF is an FDA 510(k)-cleared medical device (K760453) 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 September 12, 1976. Regulation: 8.