P-300 CAPNOGRAPH AND PULSE OXIMETER

P-300 CAPNOGRAPH AND PULSE OXIMETER is an FDA 510(k)-cleared medical device (K915773) manufactured by Pryon Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 23, 1992. Regulation: 8.