DMR/CO2 COMBO KTI

DMR/CO2 COMBO KTI is an FDA 510(k)-cleared medical device (K960468) manufactured by Nellcor Puritan Bennett, 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 April 25, 1996. Regulation: 8.