ACCUTRAX, MODEL EPF840

ACCUTRAX, MODEL EPF840 is an FDA 510(k)-cleared medical device (K982995) manufactured by Korr Medical Technologies, 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 December 3, 1998. Regulation: 8.