NAUTILUS MONOPLACE HYPERBARIC UNIT

NAUTILUS MONOPLACE HYPERBARIC UNIT is an FDA 510(k)-cleared medical device (K832127) manufactured by Nautilus Environmedical Systems, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 11, 1983. Regulation: 8.