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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.
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