KONTRON E.E.G. MONITOR, SUPERMON MODULE 7265

KONTRON E.E.G. MONITOR, SUPERMON MODULE 7265 is an FDA 510(k)-cleared medical device (K870815) manufactured by Kontron Instruments, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 31, 1988. Regulation: 8.