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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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