FDA 510(k) Applications Submitted by KATRYNA WARREN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K991784	05/25/1999	RENEW LEAD EXTENSION	ADVANCED NEUROMODULATION SYSTEMS
K032349	06/30/2003	PLACER	ADVANCED NEUROMODULATION SYSTEMS
K032034	07/01/2003	ANS AXXESS PERCUTANEOUS LEAD	ADVANCED NEUROMODULATION SYSTEMS
K191795	07/03/2019	AOCup Lens Case with AODisc	Alcon Laboratories, Inc.
K022222	07/09/2002	LAMITRODE S-SERIES (S4 AND S8) LEADS	ADVANCED NEUROMODULATION SYSTEM,INC
K052374	08/30/2005	RAPID PROGEAMMER 3.0	ADVANCED NEUROMODULATION SYSTEMS
K992946	09/01/1999	RENEW RECEIVER	ADVANCED NEUROMODULATION SYSTEMS
K173538	11/15/2017	Clear Care Cleaning & Disinfecting Solution, AOCup Lens Case with AODisc	Alcon Laboratories, Inc.
K033757	12/01/2003	MTS MULTIPROGRAM TRIAL STIMULATOR SYSTEM	ADVANCED NEUROMODULATION SYSTEMS