KONTRON KOLORMON 7250 PATIENT MONITOR

KONTRON KOLORMON 7250 PATIENT MONITOR is an FDA 510(k)-cleared medical device (K896417) manufactured by Kontron Instruments, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 11, 1989. Regulation: 8.