Integra Neurocare, LLC
Integra Neurocare, LLC appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 2, 2000.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K002392 | VENTRIX TRUE TECH VENTRICULAR TUNNELING PRESSURE MONITORING KIT, MODEL NL960-V | November 2, 2000 |
| K992006 | NEUROVIEW INSTRUMENT HOLDER, MODEL 300-33 | August 17, 1999 |
| K981246 | BEVERLY REFERENTIAL VALVE (NL850-9710) WITH INTEGRAL PERITONEAL CATHETER (NL850-9720) VALVE KIT (NL8 | May 26, 1999 |
| K973525 | MAURICE WORLDWIDE SHUNT SYSTEM | December 16, 1997 |
| K972994 | EXTERNAL CSF DRAINAGE MANAGEMENT SYSTEMS | November 3, 1997 |
| K972261 | RIVETTI-LEVINSON INSTRALUMINAL SHUNT | September 15, 1997 |
| K971617 | ENDOSCOPIC VENTRICULAR CATHETER | July 31, 1997 |
| K970983 | PERITONEAL/CARDIAC CATHETER | June 13, 1997 |
| K970658 | LUMBAR DRAINAGE ACCESSORY KIT | May 19, 1997 |
| K964371 | SHUNT TAP WITH ICP MONITORING ACCESS PORT | January 31, 1997 |
| K961859 | NOVUS STANDARD AND PEDIATRIC VALVES | December 16, 1996 |
| K963802 | SHUNT TAP | December 12, 1996 |