FDA 510(k) Applications Submitted by Christopher Phillips

FDA 510(k) Number Submission Date Device Name Applicant
K130873 03/29/2013 VWING VASCULAR NEEDLE GUIDE, 4MM X 07MM; VWING VASCULAR NEEDLE GUIDE, 6MM X 07MM; VWING VASCULAR NEEDLE GUIDE, 8MM X 07M VITAL ACCESS
K231779 06/16/2023 REMI AI Discrete Detection Module Epitel, Inc.
K243185 09/30/2024 REMI Remote EEG Monitoring System Epitel
K180560 03/01/2018 Sherlock 3CG+ T ip Confirmation System C.R. Bard, Inc.
K171348 05/08/2017 Pinpoint GT Needle Guide Kits C.R. Bard, Inc.


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