WRIGHT 1000 MONOPLACE HYPERBARIC SYSTEM

WRIGHT 1000 MONOPLACE HYPERBARIC SYSTEM is an FDA 510(k)-cleared medical device (K952545) manufactured by Wright Industries. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 27, 1997. Regulation: 8.