
Datex-Ohmeda
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AESPIRE 7900, AESPIRE VIEW is an FDA 510(k)-cleared medical device (K122445) manufactured by Datex-Ohmeda. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 11, 2012. Regulation: 8.