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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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