FDA 510(k) Applications Submitted by LORI L HAYS, MT (ASCP)

FDA 510(k) Number	Submission Date	Device Name	Applicant
K060519	02/27/2006	INTRODUCER ASSEMBLY WITH ROTATOR LOCK	TELEFLEX MEDICAL
K070561	02/27/2007	KMEDIC INTERNAL/EXTERNAL FIXATION DEVICES	TELEFLEX MEDICAL
K981246	04/06/1998	BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL850-9730)	INTEGRA NEUROCARE LLC.
K081729	06/18/2008	MODIFICATION TO GFX NERVE ABLATION SYSTEM	BIOFORM MEDICAL, INC.
K061736	06/20/2006	COMFORT FLO HUMIDIFICATION SYSTEM AND NASAL CANNULA	TELEFLEX MEDICAL
K062914	09/27/2006	HEM-O-LOK LIGATION CLIP	TELEFLEX MEDICAL
K043205	11/19/2004	RUSCH EASY TUBE	TELEFLEX MEDICAL
K063758	12/19/2006	CHONCHA THERM NEPTUNE HEATED HUMIFIER, CHONCHA THERM NEPTUNE HEATED HUMIFIER (REMANUFACTURER), MODEL# 425-00,425-00R	TELEFLEX MEDICAL
K063778	12/21/2006	FORCE FIBER POLYETHYLENE NONABSORBABLE SUTURE	TELEFLEX MEDICAL
K970983	03/18/1997	PERITONEAL/CARDIAC CATHETER	INTEGRA NEUROCARE LLC.
K971617	05/02/1997	ENDOSCOPIC VENTRICULAR CATHETER	INTEGRA NEUROCARE LLC.
K972261	06/17/1997	RIVETTI-LEVINSON INSTRALUMINAL SHUNT	INTEGRA NEUROCARE LLC.
K972994	08/12/1997	EXTERNAL CSF DRAINAGE MANAGEMENT SYSTEMS	INTEGRA NEUROCARE LLC.
K974708	12/17/1997	GEMINI STANDARD AND MINI VALVES	NEUROCARE GROUP
K973525	09/17/1997	MAURICE WORLDWIDE SHUNT SYSTEM	INTEGRA NEUROCARE LLC.