VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM

VASCULAR TECHNOLOGY UNIOX OXYGEN ALARM is an FDA 510(k)-cleared medical device (K890058) manufactured by Vascular Technology Incorporated. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 20, 1989. Regulation: 8.