KONTRON MINIMON 7134 PATIENT MONITOR

KONTRON MINIMON 7134 PATIENT MONITOR is an FDA 510(k)-cleared medical device (K844215) 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 April 3, 1985. Regulation: 8.