KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281

KONTRON CAPNOGRAPH MONITOR, SUPERMON MODULE 7281 is an FDA 510(k)-cleared medical device (K873396) manufactured by Kontron Instruments, 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 June 20, 1988. Regulation: 8.