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Neoforce Group, Inc.
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NEOPOP INFANT RESUSCITATOR WITH FLOW METER is an FDA 510(k)-cleared medical device (K102649) manufactured by Neoforce Group, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 5, 2011. Regulation: 8.