VORTRAN APM-Plus

VORTRAN APM-Plus is an FDA 510(k)-cleared medical device (K182292) manufactured by Vortran Medical Technology 1, 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 September 17, 2019. Regulation: 8.