EC 5R PLETHYSMOGRAPH

EC 5R PLETHYSMOGRAPH is an FDA 510(k)-cleared medical device (K932812) manufactured by D. E. Hokanson, 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 January 12, 1994. Regulation: 8.