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W.O.M. World of Medicine AG
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AQUILEX FLUID CONTROL SYSTEM H112 is an FDA 510(k)-cleared medical device (K112642) manufactured by W.O.M. World of Medicine AG. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 5, 2012. Regulation: 8.

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