
Datex-Ohmeda, Inc.
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DATEX-OHMEDA NETWORK AND CENTRAL is an FDA 510(k)-cleared medical device (K000647) manufactured by Datex-Ohmeda, 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 July 12, 2000. Regulation: 8.