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.