
GE Healthcare
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DATEX-OHMEDA S/5 INTERFACE MODULE E-INT is an FDA 510(k)-cleared medical device (K052880) manufactured by GE Healthcare. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 1, 2005. Regulation: 8.