Integra Neurocare, LLC is one of 15156 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Integra Neurocare, LLC - FDA 510(k) Cleared Devices
Recent clearances: NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33, BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL850-9730), MAURICE WORLDWIDE SHUNT SYSTEM
12
Total
12
Cleared
0
Denied
Integra Neurocare, LLC has 12 FDA 510(k) cleared neurology devices. Based in San Diego, US.
Historical record: 12 cleared submissions from 1996 to 2000.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Integra Neurocare, LLC
12 devices
Cleared
Nov 02, 2000
VENTRIX TRUE TECH VENTRICULAR TUNNELING PRESSURE MONITORING KIT, MODEL NL960-V
Neurology
87d
Cleared
Aug 17, 1999
NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33
Gastroenterology & Urology
63d
Cleared
May 26, 1999
BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER...
Neurology
415d
Cleared
Dec 16, 1997
MAURICE WORLDWIDE SHUNT SYSTEM
Neurology
90d
Cleared
Nov 03, 1997
EXTERNAL CSF DRAINAGE MANAGEMENT SYSTEMS
Neurology
83d
Cleared
Sep 15, 1997
RIVETTI-LEVINSON INSTRALUMINAL SHUNT
Cardiovascular
90d
Cleared
Jul 31, 1997
ENDOSCOPIC VENTRICULAR CATHETER
Neurology
90d
Cleared
Jun 13, 1997
PERITONEAL/CARDIAC CATHETER
Neurology
87d
Cleared
May 19, 1997
LUMBAR DRAINAGE ACCESSORY KIT
Neurology
87d
Cleared
Jan 31, 1997
SHUNT TAP WITH ICP MONITORING ACCESS PORT
Neurology
91d
Cleared
Dec 16, 1996
NOVUS STANDARD AND PEDIATRIC VALVES
Neurology
216d
Cleared
Dec 12, 1996
SHUNT TAP
Neurology
80d