Ventrix True Tech Ventricular Tunneling Pressure Monitoring Kit, Model NL960-V

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K002392 ↗

FDA Product Code

GWM

Device Class

Class II

Regulation

21 CFR Part 882.1620

Advisory Committee

Neurology

FDA Decision

SESE Substantially Equivalent

• Peritoneal/Cardiac Catheter

  Class II

  FDA 510(k) K970983 Active Cleared 13 Jun 1997

• Neuroview Instrument Holder, Model 300-33

  Class II

  FDA 510(k) K992006 Active Cleared 17 Aug 1999

• Beverly Referential Valve (NL850-9710) with Integral Peritoneal Catheter (NL850-9720) Valve Kit (NL850-9730)

  Class II

  FDA 510(k) K981246 Active Cleared 26 May 1999

• Novus Standard and Pediatric Valves

  Class II

  FDA 510(k) K961859 Active Cleared 16 Dec 1996

• Shunt Tap with Icp Monitoring Access Port

  Class II

  FDA 510(k) K964371 Active Cleared 31 Jan 1997

• Maurice Worldwide Shunt System

  Class II

  FDA 510(k) K973525 Active Cleared 16 Dec 1997

See all devices from Integra Neurocare, LLC →