Douglas Medical Products Inc. Receives FDA 510(k) Clearance for the TUBETECH® IV Administration Set

Wednesday, September 13, 2017

Douglas Medical Products, Inc., a growing medical device company focused on contract manufacturing of IV Administration/Extension Sets and Enteral (ENFit) Sets, announced today that it has received 510(k) clearance for TUBETECH® IV Administration Sets from the U.S. Food and Drug Administration (FDA).  TUBETECH® IV Administration Sets are cleared for use in peristaltic IV infusion pumps. This FDA clearance allows Douglas Medical Products to begin immediate commercialization of TUBETECH® IV Administration Sets for use in peristaltic IV infusion pumps.

"We are pleased to have received 510(k) clearance for the TUBETECH® IV Administration Set," stated Doug Johnson, Douglas Medical Products CEO.  "TUBETECH® technology brings new innovative solutions to current issues of IV tubing performance in peristaltic IV infusion pumps. We expect many of our customers will benefit by having TUBETECH® IV Administration Sets available for use in hospitals, alternative site settings and long-term care facilities.  The entrepreneurial mindset within Douglas Medical Products continues to bring innovative and disruptive new products to solve problems for our customers and the market place."

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