FDA 510(k) Applications Submitted by TAYSIDE FLOW TECHNOLOGIES LIMITED

FDA 510(k) Number Submission Date Device Name Applicant
K083169 10/27/2008 EPTFE SLFTM SPIRAL VASCULAR GRAFT TAYSIDE FLOW TECHNOLOGIES LIMITED
K094044 12/31/2009 SPIRAL LAMINAR FLOW VASCULAR ARTERIOVENOUS GRAFT TAYSIDE FLOW TECHNOLOGIES LIMITED


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