ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE

ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE is an FDA 510(k)-cleared medical device (K854632) manufactured by Respiratory Support Products, 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 2, 1986. Regulation: 8.