DATEX-OHMEDA NETWORK AND ICENTRAL '05, SALES REVISION 4.3

DATEX-OHMEDA NETWORK AND ICENTRAL '05, SALES REVISION 4.3 is an FDA 510(k)-cleared medical device (K052972) manufactured by GE Healthcare. 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 28, 2005. Regulation: 8.