FDA 510(k) Applications Submitted by DAVID ROBERTS

FDA 510(k) Number Submission Date Device Name Applicant
K960519 02/05/1996 MARTECH ENDOSCOPIC INJECTION NEEDLE MARTECH MEDICAL PRODUCTS, INC.
K092299 07/29/2009 TRAILBLAZER SUPPORT CATHETER EV3 INC
K162384 08/25/2016 TrailBlazer Angled Support Catheter Medtronic Vascular, Inc.(formerly ev3 Inc.)


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