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Home all news asset medical received 510(k) regulatory clearance from the u.s. food and drug administration for a range of our sterile infusion therapy products stating very high-pressure resistance of 400 psi at 10 ml/sec fluid flow

January 16, 2023

Asset Medical received 510(k) regulatory clearance from the U.S. Food and Drug Administration for a range of our Sterile Infusion Therapy Products stating very high-pressure resistance of 400 psi at 10 ml/sec fluid flow

Asset Medical received 510(k) regulatory clearance from the U.S. Food and Drug Administration for a range of our Sterile Infusion Therapy Products stating very high-pressure resistance of 400 psi at 10 ml/sec fluid flow. Our FlowArt and NeutrArt NeedleFreeConnectors and extension sets could be used in combination with devices utilized where rapid flow rates are required for infusion of intravenous fluid therapy.         

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