FDA 510(k) Applications Submitted by CHRIS PAULIK

FDA 510(k) Number Submission Date Device Name Applicant
K142383 08/26/2014 Optima XR200amx, Optima XR220amx GE Medical Systems, LLC
K162990 10/27/2016 Optima XR240amx GE Medical Systems, LLC
K173602 11/21/2017 Optima XR240amx, AutoGrid GE Medical Systems, LLC
K133664 11/29/2013 ENCORE VERSION 16 SOFTWARE FOR GE LUNAR DXA BONE DENSITOMETERS GE MEDICAL SYSTEMS ULTRASOUND & PRIMARY CARE DIAGN
K103633 12/13/2010 ACHILLES GE MEDICAL SYSTEMS CHINA CO., LTD.
K103730 12/21/2010 GE LUNAR VISCERAL FAT SOFTWARE GE MEDICAL SYSTEMS ULTRASOUND AND PRIMARY CARE DIA


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