MODEL 40-80-2 DISPOS. ESOPHAGEAL STETHO

MODEL 40-80-2 DISPOS. ESOPHAGEAL STETHO is an FDA 510(k)-cleared medical device (K823743) manufactured by Y. 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 17, 1983. Regulation: 8.