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Northwind Technologies, Corp.
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MOBILE I.V. SYSTEMS 10,20,60 is an FDA 510(k)-cleared medical device (K080695) manufactured by Northwind Technologies, Corp.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 30, 2008. Regulation: 8.

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