FDA 510(k) Applications Submitted by Phebe Varghese

FDA 510(k) Number Submission Date Device Name Applicant
K151471 06/01/2015 Radifocus Glidewire Endoscopic Wire Terumo Medical Corporation
K161546 06/03/2016 R2P SlenGuide ASHITAKA FACTORY OF TERUMO CORPORATION
K152362 08/20/2015 Terumo SurGuard 3 Safety Hypodermic Needle TERUMO (PHILIPPINES) CORPORATION
K152740 09/23/2015 Radifocus Glidewire ASHITAKA FACTORY OF TERUMO CORP.


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